13 Medical Director jobs in the United Kingdom
Medical Director
Greater London, London
HUM2N
Posted 9 days ago
Job Viewed
Job Description
Medical Director HUM2N
Summary
HUM2N is a healthcare brand which is the antidote to mainstream medicine. HUM2N launched in 2020 and currently operates out of a 4500 sq ft state-of-the-art, futuristic lounge in trendy Chelsea, London. At HUM2N, we use biology to understand your past, and cutting-edge science to transform your future. Health has traditionally been defined as “the absence of disease”, with traditional medicine solely focusing on treating symptoms. It’s time for a new era of healthcare. We believe healthcare starts when you’re healthy.
Our mission is to uncover the root causes, and resolve, prevent, and optimise our clients’ health to reach their true potential - no matter where they are on their journey.
We do this through our personalised health programmes delivered by our physician-led team, cutting-edge therapies at our HUM2N Lounge, ongoing health expert support and through our powerful range of medical-grade supplements. The HUM2N lounge offers treatments. In the future, HUM2N will scale the lounges globally and provide B2B products to clinicians that HUM2N will train in our academy.
Minimum Experience
Management & Leadership: 3 years of managing and leading clinical teams in healthcare organisations, inc CQC leadership experience, and service design.
Clinical Experience: 1 0+ years of direct clinical experience in primary or secondary care , with 5+ years of experience in Functional Medicine.
Qualifications: CCT in medical speciality egMRCGP, Functional Medicine.
Education: Delivering education to physicians and healthcare teams.
Research : Involvement in design and execution of research, published.
Medical Director
The Medical Director is a senior leadership role responsible for overseeing the medical operations and ensuring the highest standards of care and patient safety within the organization. The Medical Director plays a critical role in shaping clinical policies, driving medical strategy, and ensuring alignment with the organisation's overall goals. They will be supported by the medical board inc Director of Functional Medicine and work closely with the founder and CEO. As we seek to scale the reach of the personalised medicine we are offering.
Key Responsibilities
Medical Leadership and Strategy
- Develop and implement the clinic’s overall medical strategy, focusing on longevity, preventative care, and regenerative and functional health in conjunction with Dr Enayat.
- Establish and update clinical protocols and standard operating procedures (SOPs) to ensure consistency and quality in patient care delivery. Safeguard alignment with the latest advancements in longevity, functional, regenerative medicine, and wellness.
- Provide clinical oversight for the safe and effective use of clinic therapies
- Ensure training and development for staff is in place, with clinical performance management 121s and development plans for each client facing practitioner.
- Develop clinical team leads eg NT, clinic therapies, DC lead, aesthetic lead; and provide a system for them to be able to operate effectively in.
- Lead the clinical integration of medicine with clinic based services - aesthetics and therapies to ensure a comprehensive, patient-centred approach.
- Act as the key communicator of medical objectives to the clinic's board, administrative teams, and external stakeholders, providing strategic insights and updates on clinical performance.
Patient Care and Clinical Excellence
- Develop and oversee patient care standards, policies and protocols, ensuring they meet the highest standards of safety, effectiveness, and patient satisfaction.
- Set measurable performance indicators like client recovery times and treatment efficacy/outcome.
- Conduct client consultations, assessments, and diagnostic evaluations for patients seeking functional and longevity medicine and wellness treatments.
- Supervise the administration of treatments, particularly high-risk therapies, and ensure they adhere to regulatory standards and best practices.
- Oversee the clinical team in delivering comprehensive health plans to patients that address root causes of chronic conditions and optimise overall well-being.
Regulatory Compliance and Quality Assurance (work with Operations)
- Provide strategic oversight of clinical operations including practicing privileges and HUM2N health services, delegating day-to-day management to the clinic operations manager and department leads. Maintain oversight of quality assurance projects and audits, ensuring compliance with Care Quality Commission (CQC) standards, GDPR, and other regulatory bodies.
- Share oversight with the CEO/COO of the CQC registered Manager / Clinical Operations Manager to ensure quality assurance projects and audits are completed as per CQC requirements.
- Continuously review patient outcomes and clinical data to refine and improve care protocols.
- Develop systems to identify and mitigate clinical risks, such as adverse events or breaches of patient confidentiality.
Team Leadership and Development:
- Manage and mentor a team of practitioners, including physicians, nutritional therapists, and wellness specialists, ensuring alignment with the clinic's mission and values; and practice privileges team.
- oversee the onboarding process of health practitioners
- Provide clinical training to staff on emerging longevity-focused treatments and functional medicine protocols, and oversee training and development plans per practitioner for them to meet their JD with excellence.
- Foster a culture of continuous learning, clinical excellence, and innovation within the clinic.
- Establish and govern a framework for the ongoing evaluation for the clinical team.
Practising Privileges Doctors' Management and Governance:
- Oversee governance protocols for all practising doctors, ensuring they comply with clinic policies, UK medical standards, and continuing education requirements. Implement regular reviews and assessments to ensure the consistent quality of care provided by the medical team.
- Establish a framework for the ongoing evaluation of practising doctors.
- Regularly review and renew practising privileges, overseeing the conduction audits by the cqc registered / clinic operations manager to verify ongoing compliance with clinical and ethical standards.
- Implement robust governance policies to protect the clinic from performance issues, malpractice claims, or non-compliance among practitioners, ensuring patient safety and clinic reputation.
- Drive referrals into HUM2N services from PP through education, and engagement.
Business Development and Collaboration
- Work closely with the CEO and COO in business development to explore new opportunities for clinic growth, partnerships, and service expansion both in the UK and Internationally.
- Collaborate with external healthcare providers, insurers, and suppliers to establish partnerships that enhance service offerings and reduce costs.
- Foster relationships with academic institutions, industry leaders, and research organisations to promote clinical innovation and explore new revenue streams, such as partnerships in clinical research, product development, or industry affiliations.
Medical IT Systems and Data Integration
- Ensure that data from patient treatments, diagnostics, and wearable health technologies are effectively integrated into clinical practice to support personalised care plans and long-term health monitoring.
- Collaborate with IT and tech teams to explore emerging health technologies, such as AI-driven diagnostics, telemedicine platforms, and wearable technologies, to improve the clinic’s diagnostic capabilities and patient engagement.
- Leverage data analytics to monitor clinical performance, patient outcomes, and business metrics, translating insights into actionable strategies.
Educational Initiatives and Events
- Foster a learning environment by providing education on key wellness topics such as Longevity medicine, functional medicine, and clinic therapies offered at the clinic.
- Oversee the development of patient education, including information and instructional materials, webinars, and one-on-one consultations, to enhance patient understanding of their treatment plans and the science behind functional and longevity therapies.
- Design and implement ongoing training / educational programs.
- Spearhead community outreach programs, such as health seminars or preventive care workshops, to enhance the clinic's public profile.
- Driving and measuring medical referral quantity , quality , outcome and revenue.
Industry/ Clinic Representation
- Represent the clinic at conferences, seminars, and other industry events to promote its vision and services. Represent the clinic’s expertise and leadership in the field of functional medicine and longevity through PR, national and international media outlets, journals and more.
- Represent the clinic as a speaker at conferences, industry events, and medical symposia focused on functional medicine and HUM2N Methodology, illustrated by evidence collected (case studies, research) .
- In the absence of the CEO, serve as the on-site clinical leader, interacting directly with patients, addressing their concerns, and maintaining the clinic’s operational continuity. Ensure visibility and active engagement with both clients and staff.
Evidence, Research and Innovation
- Build body of evidence, case studies, publications, research studies, testimonials.
- Lead / collaborate on clinical research initiatives related to longevity, regenerative & functional medicine, and other innovative treatments. Partner with academic institutions, biotech firms, and industry players to develop and implement new treatments that push the boundaries of healthspan and longevity interventions.
- Ensure that new treatments and protocols introduced in the clinic are based on rigorous scientific evidence and contribute to the field of longevity and wellness.
- Partner with universities or research institutions to advance medical knowledge and contribute to peer-reviewed publications.
This advertiser has chosen not to accept applicants from your region.
0
Medical Director & Consultant Psychiatrist
Bury, South East
Cygnet
Posted 4 days ago
Job Viewed
Job Description
Job Title: Consultant Psychiatrist & Medical Director
Service & location: Cygnet Hospital Bury Hudson – Male Medium Secure Unit
Professionally Accountable to: Regional Medical Director
Managerially Responsible to: Hospital Manager
We are seeking an experienced full-time Medical Director & Consultant Psychiatrist who will work at Cygnet Hospital Bury Hudson and provide senior medical cover on Colombus ward, our 13 bed Male Medium Secure Unit
The post holder will be the Responsible Clinician and will oversee and maintain the care of all ward inpatients as required and will also have responsibility for auditing the medical services rendered at the ward and ensuring their good quality in accordance to GMC standards of good medical practice and other relevant professional guidelines.
Apart from being the Responsible Clinician, you will also be the Medical Director at Cygnet Hospital Bury Hudson
Cygnet Bury Hudson is a 78 bed hospital and provides a wide range of secure mental health services for men including individuals with a diagnosis of personality disorder.
This role is based on Columbus ward, which is a medium secure unit & delivers care for men with enduring mental health needs and co-morbidity in a calm, therapeutic environment with a focus on service user experience, shared care and safety.
This is a full-time position with 0.2 WTE as Medical Director and 0.8 WTE as Consultant Psychiatrist.
In this role, your expertise will be the driving force for life-changing treatment fully supported by a Specialty Doctor and first-class multidisciplinary team including qualified nurses, psychologist and occupational therapist.
At Cygnet, you’ll enjoy excellent professional development, shopping, travel and leisure discounts – as well as a range of healthcare and financial benefits – to support you to be happy both in and out of work.
Apply now to enjoy excellent career prospects while reaping the rewards of making a difference to others – every day.
Main duties and Responsibilities…
As a Medical Director you will:
- Ensure optimal clinical outcomes for the people in our care
- Lead on all aspects of clinical practice & serve as an example of operational excellence
- Provide leadership for medical staff on both professional and managerial issues whilst monitoring their performance
- Supervision of all consultants and ensuring consultants are supervising SDs and ASs
- Provide expert knowledge & support within the service & to the wider team
- Ensure quality & compliance with internal & external standards & regulations
- Work with colleagues to provide integrated, whole person treatment & care
- Coach, mentor & train colleagues
- Ensure regular communication and meetings with medical staff
- Assist in recruitment and retention of medical staff to provide a high quality clinical service
- Ensure that medical staff are involved in hospital clinical governance
- Work in conjunction with hospital managers to lead on the successful implementation of CQC outcomes for 4, 7 and 9
- Chair medical advisory committee meetings and attend Cygnet Medical Directors meetings
- Liaise with Responsible Officer and Regional Medical Director in respect of concerns about fitness to practice issues for medical staff
As a Consultant Psychiatrist you will:
- Lead on the provision of high quality care to the service users admitted to Colombus ward
- Act as a positive role model, maintaining and demonstrating a positive attitude towards patients, their families, visitors and other staff.
- Take overall responsibility for patient treatment plans in conjunction with the multi-disciplinary team
- Assess referrals & undertake mental state examinations of service users
- Undertake appropriate investigations, diagnosis & treatment
- Conduct ward rounds, patient reviews & clinical audits
- Lead the implementation of risk assessment, risk management & embed clinical governance within the service
- Supervise reports for Mental Health Act tribunals & managers’ hearings & attend hearings
- Liaise with the Ministry of Justice for transfer of patients and approval of leave as required
- Good maintenance of patient records
- To ensure and maintain regular communications with the Site Medical Director and Hospital Manager
- To communicate effectively through regular contact with patients, relatives, staff, directors, and any other concerned bodies; maintaining appropriate reports.
- Attend and contribute to academic meetings and adhere to the professional standards for CPD as set out by the GMC, the Department of Health and the Royal College of Psychiatrists.
- Contribute to (insert frequency) Telephone On call rota
Why Cygnet? We’ll offer you…
- Salary up to £175,000 per year
- Generous annual leave entitlement that increases with length of service
- 5 days study leave, study budget and in-house CPD/ peer group programme
- Company paid Life Assurance scheme covering 3x salary
- Contributory pension scheme
- Research opportunities to include publishing in The Cygnet Journal (Cygnet’s co-produced peer review journal) and joining the Cygnet Research & Development Group
- Teaching opportunities including teaching medical students, teaching on the Cygnet CESR programme and Cygnet MRCPsych programme
- Opportunity to lead and participate in QI & Audit initiatives
- Company Funded Cash plan with the ability to claim up to £1000 per annum worth of benefits including free Physiotherapy, Osteopaths, Optical, dental, consultations, scans and free prescriptions
- Gym Discounts across the UK as well as free online fitness classes with ClassPass, Nutritional Programmes and Fitness Consultations
- Discount schemes including Reward Gateway, NHS Discount and Blue Lights Card
- Free meals, on-site parking and EAP support
- Smart Health Toolkit, including 24 hour GP service with the option of prescription delivery to your local pharmacy
- Electric Car Scheme
We are looking for someone who is…
- Fully GMC registered & MBBS (or equivalent) qualified
- Registered on the specialist register (CCT/CESR), Section 12 and AC Status
- Experienced & knowledgeable in (insert speciality)
- Knowledgeable of the Mental Health Act and Code of Practice, along with the Mental Capacity Act 2005 and Code of Capacity
- A first-rate communicator who can interview, assess & treat patients & write clear, comprehensive medical notes
- Committed to continued professional development
- Able to work as part of a multi-disciplinary team
- A member of the Royal College of Psychiatrists (MRCPsych) or equivalent
Cygnet has been providing a national network of high-quality specialist mental health services for more than 30 years. We have built a reputation for delivering pioneering services and outstanding outcomes. Our expert care enables thousands of individuals to consistently make a positive difference to their lives.
Requirements
The successful candidate will be required to undergo an enhanced DBS and reference check and an offer of employment will be subject to successful clearance
.
What next?
If you care about making a difference – we want to talk to you.
Click the link to apply or email a copy of your CV to
This advertiser has chosen not to accept applicants from your region.
1
(Associate) Medical Director - Neurology
ThermoFisher Scientific
Posted 1 day ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
**A day in the Life:**
+ Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
+ Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
+ During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions' dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
+ Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
+ Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
+ Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
**Education**
+ MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Neurology patients in hospital practice.
**Knowledge, Skills, Abilities**
+ Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
+ Is fluent in spoken and written English
+ Shown understanding and experience with NDA submission process.
+ Shown understanding of regulatory guidelines for adverse event reporting
+ Strong communication & presentation skills and is a strong teammate
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
**A day in the Life:**
+ Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
+ Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
+ During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions' dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
+ Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
+ Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
+ Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
**Education**
+ MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Neurology patients in hospital practice.
**Knowledge, Skills, Abilities**
+ Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
+ Is fluent in spoken and written English
+ Shown understanding and experience with NDA submission process.
+ Shown understanding of regulatory guidelines for adverse event reporting
+ Strong communication & presentation skills and is a strong teammate
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
2
Medical Director, Clinical Development - Hematology/Oncology
Uxbridge, London
Gilead Sciences, Inc.
Posted 1 day ago
Job Viewed
Job Description
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
The Medical Director of Hematology/Oncology provides medical monitoring to multiple clinical trials. Additionally, the Medical Director guides the project teams to design and implement clinical studies at high quality and in a time and cost-effective manner in line with the department and corporate goals and within regulatory and resource guidelines.
**Responsibilities**
+ Provide medical monitoring to multiple hematology/oncology clinical trials
+ Lead project/study teams to design and implement hematology/oncology clinical studies
+ Write protocols, investigator brochures, clinical study reports and review clinical trial documents
+ Conduct investigator meetings and lead site initiation visits with clinical trial investigators
+ Implement and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
+ Translate findings from research and nonclinical studies into clinical development opportunities
+ Interact with clinical investigators and thought leaders
+ Work with internal regulatory affairs team and other ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines
+ Work with internal pre-clinical scientists, translational scientists, business and commercial organizations in a cross functional manner.
+ Work in a cross-functional team environment, including with clinical operations, biomarker specialists, CROs, and regulatory affairs
+ Provide clinical expertise and input for regulatory filings (i.e., BLA, MAA) as well as response to questions from regulatory authorities in the context of IND submissions, clinical trial applications or filing procedures
+ Provide clinical guidance and work in a team environment in interactions with external stakeholders (medical experts, advisory boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory, Medical Affairs, and Commercial)
**Requirements:**
+ MD/DO degree and clinical development experience in the pharmaceutical industry.
+ Board certification/specialization in Hematology or Oncology and experience managing oncology trials.
+ CAR-T therapeutic area experience (preferred)
+ Multiple myeloma disease area expertise (required)
+ Phase 2 or 3 study experience within the pharmaceutical industry.
+ Relevant drug development experience, either within industry or as a clinical investigator/physician scientist in academia, or equivalent experience.
+ Demonstrated clinical development strategist with experience designing, implementing, and conducting clinical trials, with emphasis on late-stage clinical development.
+ Knowledge of carrying out hematology/oncology clinical trials, including knowledge of hematology/oncology treatment options
+ Strategic leadership and tactical skills, excellent initiative, and judgment
+ Demonstrated ability to develop and maintain excellent working relationships with both internal colleagues and external contacts, including key thought leaders, and investigators
+ Demonstrated ability to work well in teams in a cross functional manner
+ Ability to communicate and work in a self-guided manner with scientific/technical personnel
+ Ability to think critically, and demonstrated troubleshooting and problem-solving skills
+ Self-motivated and willing to accept temporary responsibilities outside of initial job description
+ Comfortable in a dynamic small company environment with minimal direction and able to adjust workload based upon changing priorities
+ May travel up to 25%
+ Must be based in Stockley Park Gilead Office
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
The Medical Director of Hematology/Oncology provides medical monitoring to multiple clinical trials. Additionally, the Medical Director guides the project teams to design and implement clinical studies at high quality and in a time and cost-effective manner in line with the department and corporate goals and within regulatory and resource guidelines.
**Responsibilities**
+ Provide medical monitoring to multiple hematology/oncology clinical trials
+ Lead project/study teams to design and implement hematology/oncology clinical studies
+ Write protocols, investigator brochures, clinical study reports and review clinical trial documents
+ Conduct investigator meetings and lead site initiation visits with clinical trial investigators
+ Implement and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
+ Translate findings from research and nonclinical studies into clinical development opportunities
+ Interact with clinical investigators and thought leaders
+ Work with internal regulatory affairs team and other ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines
+ Work with internal pre-clinical scientists, translational scientists, business and commercial organizations in a cross functional manner.
+ Work in a cross-functional team environment, including with clinical operations, biomarker specialists, CROs, and regulatory affairs
+ Provide clinical expertise and input for regulatory filings (i.e., BLA, MAA) as well as response to questions from regulatory authorities in the context of IND submissions, clinical trial applications or filing procedures
+ Provide clinical guidance and work in a team environment in interactions with external stakeholders (medical experts, advisory boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory, Medical Affairs, and Commercial)
**Requirements:**
+ MD/DO degree and clinical development experience in the pharmaceutical industry.
+ Board certification/specialization in Hematology or Oncology and experience managing oncology trials.
+ CAR-T therapeutic area experience (preferred)
+ Multiple myeloma disease area expertise (required)
+ Phase 2 or 3 study experience within the pharmaceutical industry.
+ Relevant drug development experience, either within industry or as a clinical investigator/physician scientist in academia, or equivalent experience.
+ Demonstrated clinical development strategist with experience designing, implementing, and conducting clinical trials, with emphasis on late-stage clinical development.
+ Knowledge of carrying out hematology/oncology clinical trials, including knowledge of hematology/oncology treatment options
+ Strategic leadership and tactical skills, excellent initiative, and judgment
+ Demonstrated ability to develop and maintain excellent working relationships with both internal colleagues and external contacts, including key thought leaders, and investigators
+ Demonstrated ability to work well in teams in a cross functional manner
+ Ability to communicate and work in a self-guided manner with scientific/technical personnel
+ Ability to think critically, and demonstrated troubleshooting and problem-solving skills
+ Self-motivated and willing to accept temporary responsibilities outside of initial job description
+ Comfortable in a dynamic small company environment with minimal direction and able to adjust workload based upon changing priorities
+ May travel up to 25%
+ Must be based in Stockley Park Gilead Office
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
This advertiser has chosen not to accept applicants from your region.
3
(Senior) Medical Director - Rheumatology (Client - dedicated), EMEA
ThermoFisher Scientific
Posted 1 day ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
The Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
**A day in the Life:**
+ Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
+ Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
+ During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions' dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
+ Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
+ Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
+ Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
We would consider candidates for Senior level Medical Director who have experience in strategic development.
**Education**
+ MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Rheumatology patients in hospital practice.
**Knowledge, Skills, Abilities**
+ Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
+ Is fluent in spoken and written English
+ Shown understanding and experience with NDA submission process.
+ Shown understanding of regulatory guidelines for adverse event reporting
+ Strong communication & presentation skills and is a strong teammate
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today!** ** Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
The Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
**A day in the Life:**
+ Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials
+ Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
+ During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions' dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD, part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
+ Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications
+ Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
+ Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
We would consider candidates for Senior level Medical Director who have experience in strategic development.
**Education**
+ MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Rheumatology patients in hospital practice.
**Knowledge, Skills, Abilities**
+ Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
+ Is fluent in spoken and written English
+ Shown understanding and experience with NDA submission process.
+ Shown understanding of regulatory guidelines for adverse event reporting
+ Strong communication & presentation skills and is a strong teammate
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today!** ** Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
4
Medical Director- Oncology / Directeur Mdical en Oncologie
GE HealthCare
Posted 1 day ago
Job Viewed
Job Description
**Job Description Summary**
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Dans ce rôle, vous dirigerez la stratégie de développement clinique des produits d'imagerie moléculaire sous votre responsabilité dans le domaine de l'oncologie et de l'immuno-oncologie. Vous serez responsable de la conception et de l'exécution des plans de développement clinique à travers les activités mondiales. À ce titre, vous aurez de nombreuses interactions transversales au sein de l'entreprise, allant des fonctions précliniques aux fonctions cliniques, réglementaires et commerciales à l'échelle mondiale.
Notre activité de Diagnostic Pharmaceutique (PDx) est le principal fournisseur mondial d'agents de contraste et d'agents d'imagerie moléculaire utilisés pour améliorer les examens d'imagerie médicale. Utilisés dans toutes les principales voies de diagnostic et de traitement des maladies, les produits PDx soutiennent trois patients chaque seconde dans le monde.
**Job Description**
**Roles and Responsibilities**
+ To provide clinical leadership in cross-functional projects and product/project teams
+ To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
+ To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
+ To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
+ To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
+ To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
+ To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
+ To collaborate with multiple functions for identifying and selecting innovative products for development
+ To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
**Rôles et Responsabilités**
+ Assurer le leadership clinique dans les projets et équipes produit/projet transversaux
+ Être responsable du développement et de la validation de la stratégie médicale globale des produits assignés en collaboration avec des experts internes ou externes, et s'assurer de l'accord sur cette stratégie avec les parties prenantes internes concernées
+ Veiller à ce que les activités du projet soient planifiées, convenues et exécutées selon les jalons et le plan global de développement clinique (y compris les activités pré- et post-commercialisation)
+ Être responsable de la réalisation en temps voulu et avec précision de la documentation du projet, tels que les protocoles, les amendements, les formulaires de rapport de cas et les rapports d'étude
+ Vérifier l'exactitude scientifique des résumés sur la sécurité et l'efficacité à des fins réglementaires ou commerciales, et aider à la rédaction des sections cliniques des dossiers réglementaires ou des discussions scientifiques spécifiques aux produits, en fonction des activités pré ou post-commercialisation
+ Travailler en étroite collaboration avec les équipes de gestion des risques, de conformité, des affaires réglementaires et de pharmacovigilance pour établir et maintenir des processus solides d'évaluation et de gestion des risques pour la prise de décision
+ Contribuer aux examens de gestion des risques en ce qui concerne la sécurité des patients, à l'évaluation des risques lors de la conception des études cliniques et à l'interprétation des risques et de la sécurité des patients dans l'environnement post-commercialisation
+ Collaborer avec plusieurs fonctions pour identifier et sélectionner des produits innovants à développer
+ Travailler avec les équipes internes et les experts externes pour concevoir un plan de développement clinique et soutenir les stratégies de recherche clinique pour l'approbation réglementaire, le remboursement et l'adoption.
**Required Qualifications**
+ Medical Degree
+ Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
+ A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
+ Proven experience in Good Clinical Practice (GCP) Clinical trials
+ Must be willing to travel as required.
+ Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
**Qualifications Requises**
+ Diplôme de Médecin
+ Expérience significative dans l'industrie pharmaceutique, biotechnologique ou dans une organisation de recherche contractuelle, conduisant à une bonne compréhension du développement clinique et industriel des produits médicamenteux
+ Une expérience avérée en oncologie et immuno-oncologie (de préférence avec une expérience en diagnostic par imagerie) dans le milieu universitaire et industriel est demandée
+ Expérience confirmée des essais cliniques conformes aux Bonnes Pratiques Cliniques (BPC)
+ Disponibilité pour voyager selon les besoins
+ Expérience avec les produits Microsoft Office (Word, Excel, PowerPoint, Outlook)
**Desired Characteristics**
+ Excellent interpersonal, organization, communication, influencing skills.
+ Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
+ Experience in scientific publications/communication
+ Experience managing complex projects and/or across global regions desirable.
+ Good team player with global mindset
+ Ability to work independently and with rigor
+ Good process knowledge, experience, and skills
+ Customer savvy.
**Caractéristiques Souhaitées**
+ Excellentes compétences interpersonnelles, d'organisation, de communication et d'influence
+ Expérience dans la gestion des leaders d'opinion clés (KOL), des experts externes. Possède son propre réseau de KOLs et d'experts externes
+ Expérience dans les publications/sciences de la communication
+ Expérience dans la gestion de projets complexes et/ou dans des régions mondiales souhaitée
+ Bon esprit d'équipe avec une mentalité mondiale
+ Capacité à travailler de manière indépendante et rigoureuse
+ Bonnes connaissances et compétences en matière de processus
+ Sens du client
**Inclusion and Diversity**
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
**Behaviors**
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
**Total Rewards**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
**Inclusion et diversité**
GE HealthCare est un employeur offrant l'égalité des chances où l'inclusion compte. Les décisions relatives à l'emploi sont prises sans tenir compte de l'origine national ou ethnique, de la religion, du sexe, de l'orientation sexuelle, de l'identité ou de l'expression de genre, de l'âge, du handicap, du statut d'ancien combattant protégé ou d'autres caractéristiques protégées par la loi.
Nos rémunérations totales sont conçues pour libérer votre ambition en vous donnant la motivation et la flexibilité dont vous avez besoin pour transformer vos idées en réalités qui changent le monde. Nos salaires et nos avantages sociaux correspondent à tout ce que vous attendez d'une organisation ayant une dimension internationale, avec des possibilités de développement de carrière, dans une culture qui favorise la collaboration et le soutien.
**A propos de nous**
GE HealthCare est l'un des leaders mondiaux dans le domaine des technologies médicales et des solutions numériques. Il permet aux cliniciens de prendre des décisions plus rapides et plus pertinentes à travers des équipements intelligents, des analyses de données, des applications et des services. Avec plus de 100 ans d'expérience dans le secteur de la santé et environ 47 000 employés dans le monde, la société est au centre d'un écosystème qui travaille pour une médecine de précision.
#LI-MG1
#LI-hybrid
**Additional Information**
**Relocation Assistance Provided:** No
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Dans ce rôle, vous dirigerez la stratégie de développement clinique des produits d'imagerie moléculaire sous votre responsabilité dans le domaine de l'oncologie et de l'immuno-oncologie. Vous serez responsable de la conception et de l'exécution des plans de développement clinique à travers les activités mondiales. À ce titre, vous aurez de nombreuses interactions transversales au sein de l'entreprise, allant des fonctions précliniques aux fonctions cliniques, réglementaires et commerciales à l'échelle mondiale.
Notre activité de Diagnostic Pharmaceutique (PDx) est le principal fournisseur mondial d'agents de contraste et d'agents d'imagerie moléculaire utilisés pour améliorer les examens d'imagerie médicale. Utilisés dans toutes les principales voies de diagnostic et de traitement des maladies, les produits PDx soutiennent trois patients chaque seconde dans le monde.
**Job Description**
**Roles and Responsibilities**
+ To provide clinical leadership in cross-functional projects and product/project teams
+ To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
+ To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
+ To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
+ To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
+ To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
+ To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
+ To collaborate with multiple functions for identifying and selecting innovative products for development
+ To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
**Rôles et Responsabilités**
+ Assurer le leadership clinique dans les projets et équipes produit/projet transversaux
+ Être responsable du développement et de la validation de la stratégie médicale globale des produits assignés en collaboration avec des experts internes ou externes, et s'assurer de l'accord sur cette stratégie avec les parties prenantes internes concernées
+ Veiller à ce que les activités du projet soient planifiées, convenues et exécutées selon les jalons et le plan global de développement clinique (y compris les activités pré- et post-commercialisation)
+ Être responsable de la réalisation en temps voulu et avec précision de la documentation du projet, tels que les protocoles, les amendements, les formulaires de rapport de cas et les rapports d'étude
+ Vérifier l'exactitude scientifique des résumés sur la sécurité et l'efficacité à des fins réglementaires ou commerciales, et aider à la rédaction des sections cliniques des dossiers réglementaires ou des discussions scientifiques spécifiques aux produits, en fonction des activités pré ou post-commercialisation
+ Travailler en étroite collaboration avec les équipes de gestion des risques, de conformité, des affaires réglementaires et de pharmacovigilance pour établir et maintenir des processus solides d'évaluation et de gestion des risques pour la prise de décision
+ Contribuer aux examens de gestion des risques en ce qui concerne la sécurité des patients, à l'évaluation des risques lors de la conception des études cliniques et à l'interprétation des risques et de la sécurité des patients dans l'environnement post-commercialisation
+ Collaborer avec plusieurs fonctions pour identifier et sélectionner des produits innovants à développer
+ Travailler avec les équipes internes et les experts externes pour concevoir un plan de développement clinique et soutenir les stratégies de recherche clinique pour l'approbation réglementaire, le remboursement et l'adoption.
**Required Qualifications**
+ Medical Degree
+ Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
+ A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
+ Proven experience in Good Clinical Practice (GCP) Clinical trials
+ Must be willing to travel as required.
+ Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
**Qualifications Requises**
+ Diplôme de Médecin
+ Expérience significative dans l'industrie pharmaceutique, biotechnologique ou dans une organisation de recherche contractuelle, conduisant à une bonne compréhension du développement clinique et industriel des produits médicamenteux
+ Une expérience avérée en oncologie et immuno-oncologie (de préférence avec une expérience en diagnostic par imagerie) dans le milieu universitaire et industriel est demandée
+ Expérience confirmée des essais cliniques conformes aux Bonnes Pratiques Cliniques (BPC)
+ Disponibilité pour voyager selon les besoins
+ Expérience avec les produits Microsoft Office (Word, Excel, PowerPoint, Outlook)
**Desired Characteristics**
+ Excellent interpersonal, organization, communication, influencing skills.
+ Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
+ Experience in scientific publications/communication
+ Experience managing complex projects and/or across global regions desirable.
+ Good team player with global mindset
+ Ability to work independently and with rigor
+ Good process knowledge, experience, and skills
+ Customer savvy.
**Caractéristiques Souhaitées**
+ Excellentes compétences interpersonnelles, d'organisation, de communication et d'influence
+ Expérience dans la gestion des leaders d'opinion clés (KOL), des experts externes. Possède son propre réseau de KOLs et d'experts externes
+ Expérience dans les publications/sciences de la communication
+ Expérience dans la gestion de projets complexes et/ou dans des régions mondiales souhaitée
+ Bon esprit d'équipe avec une mentalité mondiale
+ Capacité à travailler de manière indépendante et rigoureuse
+ Bonnes connaissances et compétences en matière de processus
+ Sens du client
**Inclusion and Diversity**
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
**Behaviors**
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
**Total Rewards**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
**Inclusion et diversité**
GE HealthCare est un employeur offrant l'égalité des chances où l'inclusion compte. Les décisions relatives à l'emploi sont prises sans tenir compte de l'origine national ou ethnique, de la religion, du sexe, de l'orientation sexuelle, de l'identité ou de l'expression de genre, de l'âge, du handicap, du statut d'ancien combattant protégé ou d'autres caractéristiques protégées par la loi.
Nos rémunérations totales sont conçues pour libérer votre ambition en vous donnant la motivation et la flexibilité dont vous avez besoin pour transformer vos idées en réalités qui changent le monde. Nos salaires et nos avantages sociaux correspondent à tout ce que vous attendez d'une organisation ayant une dimension internationale, avec des possibilités de développement de carrière, dans une culture qui favorise la collaboration et le soutien.
**A propos de nous**
GE HealthCare est l'un des leaders mondiaux dans le domaine des technologies médicales et des solutions numériques. Il permet aux cliniciens de prendre des décisions plus rapides et plus pertinentes à travers des équipements intelligents, des analyses de données, des applications et des services. Avec plus de 100 ans d'expérience dans le secteur de la santé et environ 47 000 employés dans le monde, la société est au centre d'un écosystème qui travaille pour une médecine de précision.
#LI-MG1
#LI-hybrid
**Additional Information**
**Relocation Assistance Provided:** No
This advertiser has chosen not to accept applicants from your region.
5
Medical Director- Oncology / Directeur Mdical en Oncologie
Chalfont St Giles, South East
GE HealthCare
Posted 1 day ago
Job Viewed
Job Description
**Job Description Summary**
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Dans ce rôle, vous dirigerez la stratégie de développement clinique des produits d'imagerie moléculaire sous votre responsabilité dans le domaine de l'oncologie et de l'immuno-oncologie. Vous serez responsable de la conception et de l'exécution des plans de développement clinique à travers les activités mondiales. À ce titre, vous aurez de nombreuses interactions transversales au sein de l'entreprise, allant des fonctions précliniques aux fonctions cliniques, réglementaires et commerciales à l'échelle mondiale.
Notre activité de Diagnostic Pharmaceutique (PDx) est le principal fournisseur mondial d'agents de contraste et d'agents d'imagerie moléculaire utilisés pour améliorer les examens d'imagerie médicale. Utilisés dans toutes les principales voies de diagnostic et de traitement des maladies, les produits PDx soutiennent trois patients chaque seconde dans le monde.
**Job Description**
**Roles and Responsibilities**
+ To provide clinical leadership in cross-functional projects and product/project teams
+ To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
+ To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
+ To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
+ To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
+ To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
+ To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
+ To collaborate with multiple functions for identifying and selecting innovative products for development
+ To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
**Rôles et Responsabilités**
+ Assurer le leadership clinique dans les projets et équipes produit/projet transversaux
+ Être responsable du développement et de la validation de la stratégie médicale globale des produits assignés en collaboration avec des experts internes ou externes, et s'assurer de l'accord sur cette stratégie avec les parties prenantes internes concernées
+ Veiller à ce que les activités du projet soient planifiées, convenues et exécutées selon les jalons et le plan global de développement clinique (y compris les activités pré- et post-commercialisation)
+ Être responsable de la réalisation en temps voulu et avec précision de la documentation du projet, tels que les protocoles, les amendements, les formulaires de rapport de cas et les rapports d'étude
+ Vérifier l'exactitude scientifique des résumés sur la sécurité et l'efficacité à des fins réglementaires ou commerciales, et aider à la rédaction des sections cliniques des dossiers réglementaires ou des discussions scientifiques spécifiques aux produits, en fonction des activités pré ou post-commercialisation
+ Travailler en étroite collaboration avec les équipes de gestion des risques, de conformité, des affaires réglementaires et de pharmacovigilance pour établir et maintenir des processus solides d'évaluation et de gestion des risques pour la prise de décision
+ Contribuer aux examens de gestion des risques en ce qui concerne la sécurité des patients, à l'évaluation des risques lors de la conception des études cliniques et à l'interprétation des risques et de la sécurité des patients dans l'environnement post-commercialisation
+ Collaborer avec plusieurs fonctions pour identifier et sélectionner des produits innovants à développer
+ Travailler avec les équipes internes et les experts externes pour concevoir un plan de développement clinique et soutenir les stratégies de recherche clinique pour l'approbation réglementaire, le remboursement et l'adoption.
**Required Qualifications**
+ Medical Degree
+ Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
+ A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
+ Proven experience in Good Clinical Practice (GCP) Clinical trials
+ Must be willing to travel as required.
+ Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
**Qualifications Requises**
+ Diplôme de Médecin
+ Expérience significative dans l'industrie pharmaceutique, biotechnologique ou dans une organisation de recherche contractuelle, conduisant à une bonne compréhension du développement clinique et industriel des produits médicamenteux
+ Une expérience avérée en oncologie et immuno-oncologie (de préférence avec une expérience en diagnostic par imagerie) dans le milieu universitaire et industriel est demandée
+ Expérience confirmée des essais cliniques conformes aux Bonnes Pratiques Cliniques (BPC)
+ Disponibilité pour voyager selon les besoins
+ Expérience avec les produits Microsoft Office (Word, Excel, PowerPoint, Outlook)
**Desired Characteristics**
+ Excellent interpersonal, organization, communication, influencing skills.
+ Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
+ Experience in scientific publications/communication
+ Experience managing complex projects and/or across global regions desirable.
+ Good team player with global mindset
+ Ability to work independently and with rigor
+ Good process knowledge, experience, and skills
+ Customer savvy.
**Caractéristiques Souhaitées**
+ Excellentes compétences interpersonnelles, d'organisation, de communication et d'influence
+ Expérience dans la gestion des leaders d'opinion clés (KOL), des experts externes. Possède son propre réseau de KOLs et d'experts externes
+ Expérience dans les publications/sciences de la communication
+ Expérience dans la gestion de projets complexes et/ou dans des régions mondiales souhaitée
+ Bon esprit d'équipe avec une mentalité mondiale
+ Capacité à travailler de manière indépendante et rigoureuse
+ Bonnes connaissances et compétences en matière de processus
+ Sens du client
**Inclusion and Diversity**
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
**Behaviors**
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
**Total Rewards**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
**Inclusion et diversité**
GE HealthCare est un employeur offrant l'égalité des chances où l'inclusion compte. Les décisions relatives à l'emploi sont prises sans tenir compte de l'origine national ou ethnique, de la religion, du sexe, de l'orientation sexuelle, de l'identité ou de l'expression de genre, de l'âge, du handicap, du statut d'ancien combattant protégé ou d'autres caractéristiques protégées par la loi.
Nos rémunérations totales sont conçues pour libérer votre ambition en vous donnant la motivation et la flexibilité dont vous avez besoin pour transformer vos idées en réalités qui changent le monde. Nos salaires et nos avantages sociaux correspondent à tout ce que vous attendez d'une organisation ayant une dimension internationale, avec des possibilités de développement de carrière, dans une culture qui favorise la collaboration et le soutien.
**A propos de nous**
GE HealthCare est l'un des leaders mondiaux dans le domaine des technologies médicales et des solutions numériques. Il permet aux cliniciens de prendre des décisions plus rapides et plus pertinentes à travers des équipements intelligents, des analyses de données, des applications et des services. Avec plus de 100 ans d'expérience dans le secteur de la santé et environ 47 000 employés dans le monde, la société est au centre d'un écosystème qui travaille pour une médecine de précision.
#LI-MG1
#LI-hybrid
**Additional Information**
**Relocation Assistance Provided:** No
In this role, you will be leading the clinical development strategy of Molecular Imaging products under your responsibility in the Oncology and Immune-oncology domain. You will be responsible for designing and executing clinical development plans across the global businesses. As such, individual will have extensive cross-functional interaction within the Company, ranging from pre-clinical through to clinical, regulatory and commercial functions worldwide.
Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.
Dans ce rôle, vous dirigerez la stratégie de développement clinique des produits d'imagerie moléculaire sous votre responsabilité dans le domaine de l'oncologie et de l'immuno-oncologie. Vous serez responsable de la conception et de l'exécution des plans de développement clinique à travers les activités mondiales. À ce titre, vous aurez de nombreuses interactions transversales au sein de l'entreprise, allant des fonctions précliniques aux fonctions cliniques, réglementaires et commerciales à l'échelle mondiale.
Notre activité de Diagnostic Pharmaceutique (PDx) est le principal fournisseur mondial d'agents de contraste et d'agents d'imagerie moléculaire utilisés pour améliorer les examens d'imagerie médicale. Utilisés dans toutes les principales voies de diagnostic et de traitement des maladies, les produits PDx soutiennent trois patients chaque seconde dans le monde.
**Job Description**
**Roles and Responsibilities**
+ To provide clinical leadership in cross-functional projects and product/project teams
+ To be responsible for the development and validation of the overall medical strategy of the assigned product(s) with appropriate internal or external experts, and for the agreement on this strategy with the appropriate internal business stakeholders
+ To be responsible that project activities are planned, agreed and executed according to the milestones and the overall clinical development plan (it includes pre- and post-marketing activities)
+ To be responsible for the timely and accurate completion of project documentation such as protocols, amendments, case report forms and study reports
+ To verify scientific accuracy of safety and efficacy summaries for regulatory/commercial purposes and to assist with the clinical sections of regulatory dossiers and or product specific scientific discussion, depending on pre or post-marketing activities
+ To work closely with the Risk Management, Compliance, Regulatory Affairs and Pharmacovigilance teams to establish and maintain strong risk assessment and management processes for decision making
+ To provide input into Risk Management reviews as it relates to patient safety, the performance of risk assessment in the design of clinical studies, and the interpretation of patient safety and risk in the post-market environment
+ To collaborate with multiple functions for identifying and selecting innovative products for development
+ To work with internal teams and external experts to design clinical development plan and to support clinical research strategies for regulatory approval, reimbursement and adoption.
**Rôles et Responsabilités**
+ Assurer le leadership clinique dans les projets et équipes produit/projet transversaux
+ Être responsable du développement et de la validation de la stratégie médicale globale des produits assignés en collaboration avec des experts internes ou externes, et s'assurer de l'accord sur cette stratégie avec les parties prenantes internes concernées
+ Veiller à ce que les activités du projet soient planifiées, convenues et exécutées selon les jalons et le plan global de développement clinique (y compris les activités pré- et post-commercialisation)
+ Être responsable de la réalisation en temps voulu et avec précision de la documentation du projet, tels que les protocoles, les amendements, les formulaires de rapport de cas et les rapports d'étude
+ Vérifier l'exactitude scientifique des résumés sur la sécurité et l'efficacité à des fins réglementaires ou commerciales, et aider à la rédaction des sections cliniques des dossiers réglementaires ou des discussions scientifiques spécifiques aux produits, en fonction des activités pré ou post-commercialisation
+ Travailler en étroite collaboration avec les équipes de gestion des risques, de conformité, des affaires réglementaires et de pharmacovigilance pour établir et maintenir des processus solides d'évaluation et de gestion des risques pour la prise de décision
+ Contribuer aux examens de gestion des risques en ce qui concerne la sécurité des patients, à l'évaluation des risques lors de la conception des études cliniques et à l'interprétation des risques et de la sécurité des patients dans l'environnement post-commercialisation
+ Collaborer avec plusieurs fonctions pour identifier et sélectionner des produits innovants à développer
+ Travailler avec les équipes internes et les experts externes pour concevoir un plan de développement clinique et soutenir les stratégies de recherche clinique pour l'approbation réglementaire, le remboursement et l'adoption.
**Required Qualifications**
+ Medical Degree
+ Substantial experience in Pharmaceutical, Biotech, or Contract Research Organization leading to good understanding of Clinical and Industry development of drug products.
+ A proven practice in Oncology and Immune oncology (preferably with Imaging diagnostic experience) in both academia and industry is requested.
+ Proven experience in Good Clinical Practice (GCP) Clinical trials
+ Must be willing to travel as required.
+ Experience working with Microsoft office products (Word, Excel, PowerPoint, Outlook)
**Qualifications Requises**
+ Diplôme de Médecin
+ Expérience significative dans l'industrie pharmaceutique, biotechnologique ou dans une organisation de recherche contractuelle, conduisant à une bonne compréhension du développement clinique et industriel des produits médicamenteux
+ Une expérience avérée en oncologie et immuno-oncologie (de préférence avec une expérience en diagnostic par imagerie) dans le milieu universitaire et industriel est demandée
+ Expérience confirmée des essais cliniques conformes aux Bonnes Pratiques Cliniques (BPC)
+ Disponibilité pour voyager selon les besoins
+ Expérience avec les produits Microsoft Office (Word, Excel, PowerPoint, Outlook)
**Desired Characteristics**
+ Excellent interpersonal, organization, communication, influencing skills.
+ Experience in managing KOLs, external experts. Brings his/her own network of KOLs, external experts.
+ Experience in scientific publications/communication
+ Experience managing complex projects and/or across global regions desirable.
+ Good team player with global mindset
+ Ability to work independently and with rigor
+ Good process knowledge, experience, and skills
+ Customer savvy.
**Caractéristiques Souhaitées**
+ Excellentes compétences interpersonnelles, d'organisation, de communication et d'influence
+ Expérience dans la gestion des leaders d'opinion clés (KOL), des experts externes. Possède son propre réseau de KOLs et d'experts externes
+ Expérience dans les publications/sciences de la communication
+ Expérience dans la gestion de projets complexes et/ou dans des régions mondiales souhaitée
+ Bon esprit d'équipe avec une mentalité mondiale
+ Capacité à travailler de manière indépendante et rigoureuse
+ Bonnes connaissances et compétences en matière de processus
+ Sens du client
**Inclusion and Diversity**
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
**Behaviors**
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
**Total Rewards**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
**Inclusion et diversité**
GE HealthCare est un employeur offrant l'égalité des chances où l'inclusion compte. Les décisions relatives à l'emploi sont prises sans tenir compte de l'origine national ou ethnique, de la religion, du sexe, de l'orientation sexuelle, de l'identité ou de l'expression de genre, de l'âge, du handicap, du statut d'ancien combattant protégé ou d'autres caractéristiques protégées par la loi.
Nos rémunérations totales sont conçues pour libérer votre ambition en vous donnant la motivation et la flexibilité dont vous avez besoin pour transformer vos idées en réalités qui changent le monde. Nos salaires et nos avantages sociaux correspondent à tout ce que vous attendez d'une organisation ayant une dimension internationale, avec des possibilités de développement de carrière, dans une culture qui favorise la collaboration et le soutien.
**A propos de nous**
GE HealthCare est l'un des leaders mondiaux dans le domaine des technologies médicales et des solutions numériques. Il permet aux cliniciens de prendre des décisions plus rapides et plus pertinentes à travers des équipements intelligents, des analyses de données, des applications et des services. Avec plus de 100 ans d'expérience dans le secteur de la santé et environ 47 000 employés dans le monde, la société est au centre d'un écosystème qui travaille pour une médecine de précision.
#LI-MG1
#LI-hybrid
**Additional Information**
**Relocation Assistance Provided:** No
This advertiser has chosen not to accept applicants from your region.
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6
Scientific Director – Medical Communications
London, London
Meet Life Sciences
Posted 9 days ago
Job Viewed
Job Description
Join a Leading Medical Communications Agency as a Scientific Director
We’re looking for an experienced and driven Scientific Director (SD) to join our dynamic and rapidly growing team. If you're passionate about scientific storytelling, thrive in a fast-paced agency environment, and are ready to make an immediate impact, this role is for you.
This is a rare opportunity to step into a senior-level role with strategic oversight and leadership responsibilities across publications, medical affairs, and commercial projects. You’ll play a key part in shaping the direction of high-profile accounts and mentoring the next generation of scientific talent.
What You’ll Be Doing
Project Focus:
- Publications (50%) – Drive strategic and tactical publications planning and execution across key accounts.
- Medical Affairs (40%) – Support medical strategy development and deliver engaging, scientifically robust materials.
- Commercial (10%) – Contribute to promotional content with scientific rigor and commercial insight.
Your Core Responsibilities Will Include:
- Leading the scientific strategy, content development, and client interactions across a range of therapeutic areas, with a primary focus in neuroscience/psychiatry .
- Collaborating closely with client services and creative teams to deliver high-quality, scientifically accurate materials.
- Presenting confidently to clients, including at onsite meetings and advisory boards.
- Supporting new business development, including proposal writing and pitch presentations.
- Mentoring and managing a team of writers, providing guidance, feedback, and review support.
- Ensuring delivery excellence and scientific accuracy across all outputs.
- Driving internal innovation and thought leadership in medical communications best practices.
What We’re Looking For
- 6+ years of medical writing experience in an agency or pharma setting, ideally spanning multiple therapy areas and deliverables.
- Proven leadership skills – including team management, project oversight, and internal mentorship.
- Experience presenting scientific material to clients and key opinion leaders.
- Deep understanding of strategic publication and medical affairs planning.
- Strong commercial awareness and experience managing budgets and timelines.
- Excellent communication and interpersonal skills, with a knack for translating complex science into compelling content.
- Proficiency in MS Word and PowerPoint.
- Comfortable working both independently and as part of a collaborative cross-functional team.
Why Join Us?
- Strategic Influence: Be a key player in shaping the future of our scientific offering and client relationships.
- Supportive Environment: Work in a collaborative and creative agency culture that values innovation and thought leadership.
- Flexible Working: Hybrid working model, with full remote flexibility if commuting time exceeds 1.5 hours.
- Career Growth: Exposure to diverse project types, clients, and business development opportunities.
- Therapeutic Impact: Focus on meaningful work in neuroscience/psychiatry – areas where your expertise can truly make a difference.
Ready to make a move that matters?
We’re hiring urgently to meet growing client demand and are looking for someone who can hit the ground running and lead with both scientific rigor and heart.
This advertiser has chosen not to accept applicants from your region.
7
Scientific Director – Medical Communications
Meet Life Sciences
Posted 9 days ago
Job Viewed
Job Description
Join a Leading Medical Communications Agency as a Scientific Director
We’re looking for an experienced and driven Scientific Director (SD) to join our dynamic and rapidly growing team. If you're passionate about scientific storytelling, thrive in a fast-paced agency environment, and are ready to make an immediate impact, this role is for you.
This is a rare opportunity to step into a senior-level role with strategic oversight and leadership responsibilities across publications, medical affairs, and commercial projects. You’ll play a key part in shaping the direction of high-profile accounts and mentoring the next generation of scientific talent.
What You’ll Be Doing
Project Focus:
- Publications (50%) – Drive strategic and tactical publications planning and execution across key accounts.
- Medical Affairs (40%) – Support medical strategy development and deliver engaging, scientifically robust materials.
- Commercial (10%) – Contribute to promotional content with scientific rigor and commercial insight.
Your Core Responsibilities Will Include:
- Leading the scientific strategy, content development, and client interactions across a range of therapeutic areas, with a primary focus in neuroscience/psychiatry .
- Collaborating closely with client services and creative teams to deliver high-quality, scientifically accurate materials.
- Presenting confidently to clients, including at onsite meetings and advisory boards.
- Supporting new business development, including proposal writing and pitch presentations.
- Mentoring and managing a team of writers, providing guidance, feedback, and review support.
- Ensuring delivery excellence and scientific accuracy across all outputs.
- Driving internal innovation and thought leadership in medical communications best practices.
What We’re Looking For
- 6+ years of medical writing experience in an agency or pharma setting, ideally spanning multiple therapy areas and deliverables.
- Proven leadership skills – including team management, project oversight, and internal mentorship.
- Experience presenting scientific material to clients and key opinion leaders.
- Deep understanding of strategic publication and medical affairs planning.
- Strong commercial awareness and experience managing budgets and timelines.
- Excellent communication and interpersonal skills, with a knack for translating complex science into compelling content.
- Proficiency in MS Word and PowerPoint.
- Comfortable working both independently and as part of a collaborative cross-functional team.
Why Join Us?
- Strategic Influence: Be a key player in shaping the future of our scientific offering and client relationships.
- Supportive Environment: Work in a collaborative and creative agency culture that values innovation and thought leadership.
- Flexible Working: Hybrid working model, with full remote flexibility if commuting time exceeds 1.5 hours.
- Career Growth: Exposure to diverse project types, clients, and business development opportunities.
- Therapeutic Impact: Focus on meaningful work in neuroscience/psychiatry – areas where your expertise can truly make a difference.
Ready to make a move that matters?
We’re hiring urgently to meet growing client demand and are looking for someone who can hit the ground running and lead with both scientific rigor and heart.
This advertiser has chosen not to accept applicants from your region.
8
Director, Medical Strategy Lead - Cardiovascular
London, London
IQVIA
Posted 1 day ago
Job Viewed
Job Description
IQVIA Cardiovascular Center of Excellence, a hub of Cardiovascular clinical innovation, is is looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help us expand our Cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development.
The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA.
The key remit of the role is drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials.
The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials and studies. The Medical Strategy Lead will also be responsible for early engagement business development activities, providing scientific knowledge and expertise to guide sponsors in Cardiovascular development.
As a subject matter expert, the Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.
**RESPONSIBILITIES:**
+ Accountable and responsible for creating innovative, evidence-based, and patient-centered delivery strategies and solutions for Cardiovascular trials or studies, addressing the specific needs and challenges of each customer.
+ In partnership with Indication-Specific Medical Strategy, Operations, Sales, and other functions, responsible for award of strategic and tactical new business to achieve annual Gross New Business targets. Responsible for the inclusion of Cardiovascular elements into proposals.
+ Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
+ Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required.
+ Participates in strategic business development activities including presentations to prospective clients and professional meetings.
+ Maintains awareness of industry pipeline and scientific and business landscape; supports due diligence research of the Cardiovascular landscape.
**REQUIREMENTS:**
_Scientific and Research Qualifications and Experience_
+ **Cardiologist.** A degree from an accredited and internationally recognized school is required
+ 2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience
+ Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular
+ Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
+ In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall offering
+ Strong clinical research skills and commitment to evidence-based and patient-centered clinical development
_Professional Skills_
+ Excellent communication, presentation and interpersonal skills, including good command of English language (both written and spoken)
+ Strong leadership skills, ability to work with minimal supervision, and lead a virtual team in a matrix organization
+ Innovative and strategic thinker
+ Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in both sales and operational environments
+ Flexible and able to work in situations where specifications may or may not be well defined and willing to support work in other therapeutic areas when required
+ Confident and capable in the use of technology, applications and other media e.g. databases and internet to research assess new opportunities, maintain currency of therapeutic and operational knowledge and competitive landscape.
+ Proven ability to make decisions with limited information, bringing clarity to disparate information to inform actions and drive results
_Interpersonal Skills_
+ Ability to establish and maintain effective working relationships with coworkers, managers and clients. Maintains a positive outlook at work; handles criticism well and learns from it
+ Ability to establish and maintain effective working relationships with a wide network of individuals e.g. coworkers, managers and customers
+ Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA.
The key remit of the role is drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/her clinical, scientific, and operational knowledge to harness the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials.
The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials and studies. The Medical Strategy Lead will also be responsible for early engagement business development activities, providing scientific knowledge and expertise to guide sponsors in Cardiovascular development.
As a subject matter expert, the Medical Strategy Lead will drive thought leadership activities including presentations, publications, and interactions with the medical scientific community.
**RESPONSIBILITIES:**
+ Accountable and responsible for creating innovative, evidence-based, and patient-centered delivery strategies and solutions for Cardiovascular trials or studies, addressing the specific needs and challenges of each customer.
+ In partnership with Indication-Specific Medical Strategy, Operations, Sales, and other functions, responsible for award of strategic and tactical new business to achieve annual Gross New Business targets. Responsible for the inclusion of Cardiovascular elements into proposals.
+ Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
+ Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required.
+ Participates in strategic business development activities including presentations to prospective clients and professional meetings.
+ Maintains awareness of industry pipeline and scientific and business landscape; supports due diligence research of the Cardiovascular landscape.
**REQUIREMENTS:**
_Scientific and Research Qualifications and Experience_
+ **Cardiologist.** A degree from an accredited and internationally recognized school is required
+ 2+ years clinical research relevant experience, including hands on operational delivery and/or drug development experience
+ Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiovascular
+ Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
+ In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall offering
+ Strong clinical research skills and commitment to evidence-based and patient-centered clinical development
_Professional Skills_
+ Excellent communication, presentation and interpersonal skills, including good command of English language (both written and spoken)
+ Strong leadership skills, ability to work with minimal supervision, and lead a virtual team in a matrix organization
+ Innovative and strategic thinker
+ Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in both sales and operational environments
+ Flexible and able to work in situations where specifications may or may not be well defined and willing to support work in other therapeutic areas when required
+ Confident and capable in the use of technology, applications and other media e.g. databases and internet to research assess new opportunities, maintain currency of therapeutic and operational knowledge and competitive landscape.
+ Proven ability to make decisions with limited information, bringing clarity to disparate information to inform actions and drive results
_Interpersonal Skills_
+ Ability to establish and maintain effective working relationships with coworkers, managers and clients. Maintains a positive outlook at work; handles criticism well and learns from it
+ Ability to establish and maintain effective working relationships with a wide network of individuals e.g. coworkers, managers and customers
+ Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
9