80 Medical Director jobs in the United Kingdom

Global Medical Affairs Director

London, London Novartis Farmacéutica

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Job Description

#LI-Hybrid 12 days per month on-site
Location: London, United Kingdom & Barcelona, Spain
Are you ready to shape the global medical voice across the asset lifecycle? Our Global Medical Affairs team is at the forefront of enterprise-wide medical leadership, driving strategy across therapeutic areas and ensuring a unified international and U.S. medical perspective. We lead the development and ownership of Integrated Evidence Packages (IEPs), guiding innovative evidence generation through interventional studies, non-interventional studies (NIS), real-world evidence (RWE), and implementation science projects.
This is a unique opportunity to bring your deep expertise in drug development and scientific strategy to some of the most complex and high-impact programs in the industry. You’ll act as a subject matter expert, influencing design and execution across disease areas, and providing strategic leadership in collaboration with NIBR, Development, and Medical Affairs teams globally. If you're passionate about advancing medical innovation and thrive in high-stakes, cross-functional environments—this role is for you.

About the Role

Key responsibilities:

  • Lead development and execution of medical affairs strategy for Asset priority programs, including transformative tactics such as research/population health, innovative partnerships, and integrated evidence plans.
  • Co-develop plans for evidence generation, MSL / Field Medical Affairs strategy, medical education programs, scientific publication planning, and Medical Expert network development.
  • Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders.
  • Track financials to ensure timely and cost-effective development and execution of medical activities.
  • Prepare SRC submissions for TA assets within remit.
  • Partner with Development, US and International cross-functional teams to shape the portfolio early and diversify evidence to achieve broad access at launch and enhance impact on clinical practice for priority programs.
  • Represent Global Medical Affairs around prioritized portfolio with internal and external audiences, in collaboration with TAs, including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners.
  • Advocate for “the voice of the patient” internally and evaluate factors relevant to a patient’s informed decision-making.
  • Provide direction and input into the development and implementation of successful reimbursement and market-access strategies.
  • Contribute proactive input to Development on potential new therapeutic indications to enrich Registration Programs and explore new therapeutic opportunities.
  • Fluent oral and written English.
  • PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to discipline for which you will be responsible is an advantage.
  • Experience in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development.
  • Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change.
  • Deep understanding of health care systems and key external stakeholders.
  • Strong track record of delivery focus for time and quality in medical affairs projects.
  • Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination.
  • Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities.

Commitment to Diversity and Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up:

GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

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Medical Director

Birmingham, West Midlands Birmingham Hospice

Posted 10 days ago

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Job Description

Medical Director – Birmingham Hospice

Location: Selly Park and Erdington, Birmingham


Salary: Competitive Salary based on an 18.75 hours per week commitment plus on-call allowances


Contract: Permanent, part-time - Flexible working is an option that can be discussed


Reporting to: Chief Executive Officer


Woodrow Mercer Healthcare have been retained to identify a visionary and values-led medical professional to join Birmingham Hospice, a special organisation that directly cares for up to 1,000 people every day across Birmingham and Sandwell.

Our teams consist of dedicated professionals, committed to helping people through some of the most important and difficult moments, offering exceptional palliative and end of life care with warmth, dignity and compassion- supporting everyday needs.


This is not just a leadership role, it is a chance to make significant impacts upon lives who are most in need, within an organisation that places those people at its heart. You will lead and nurture a dedicated medical team, helping shape the strategic direction of the hospice by working closely with partners across health and social care so that every person in our community has access to the care they deserve. You will have autonomy and responsibility for leading medical education & training teams and become the accountable officer for controlled drugs. This is a truly holistic role for a medical professional willing to develop their portfolio and experience in a supportive environment.


Why join Birmingham Hospice?


Birmingham Hospice is the leading provider of palliative and end of life care in the region, operating from Selly Park and Erdington, as well as delivering home care services. Birmingham Hospice is enriched in history, formed through the merger of Birmingham St Mary’s and John Taylor Hospices. This is a history we are very proud of at Birmingham Hospice, which we hope to build upon by expanding our care services across the westmidlands in partnership with aligned individuals, who carry the same vision of supporting those in need of care.


Our values of Kindness, Respect, Positivity, Togetherness, Openness and Innovation shape every decision we make- bringing these values to every interaction we have. We believe in creating a culture where everyone feels valued, heard and supported to push themselves to be their best versions.


Requirements


We are seeking a compassionate and collaborative leader who can bring both expertise and empathy to the role.


Requirements for the role are as follows:


  • GMC registration and ideally experience of or a least a curiosity & commitment to build experience in palliative or end of life care
  • A track record of inspiring, supporting and empowering multi-professional teams
  • The ability to build trusting relationships and foster strong partnerships across the NHS, charity sector and local communities
  • A commitment to inclusive and equitable care for all
  • A thoughtful approach to clinical governance, strategy and service improvement


You need to be someone who leads with kindness, ensuring you listen empathetically to patient’s needs, bringing a supportive nature to all day-to-day tasks. Equally you need to be as comfortable connecting with families throughout care processes as you are contributing your voice to strategic discussions at board level- as care requirements go beyond solely patient care, we pride ourselves on offering the needed support throughout every step of our care cycle to those closest to our patients- making life as easy as possible.


What we offer


  • 35 days holiday plus bank holidays (pro-rata)
  • Generous pension options, including the ability to retain your NHS pension
  • Flexible working to help you balance your personal and professional life
  • Opportunities for learning, development and leadership coaching
  • Free parking, refreshments and on-site cafés at both sites


At Birmingham Hospice, your leadership will make a lasting and meaningful difference. You will be pushed to grow both personally and professionally within our teams, where supporting one another is encouraged to work towards a common goal of helping create an environment where patients and their loved ones feel safe and supported- enabling us to provide the care people deserve.


How to apply


For an informal and confidential discussion, please contact:

Sam Alsop-Hall – or call 07940240585

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Medical Director

London, London Cactus Communications

Posted 1 day ago

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Job Description

Overview

Cactus Life Sciences partners with the global biopharma industry to drive innovation and elevate patient outcomes through agile, science-driven medical communications. We transform complex data into actionable insights, bridging the critical gaps between research, decision-making, and real-world healthcare impact. As a growing scientific communications agency, we are seeking a self-motivated, strategy-oriented Medical Director to add to our scientific services team.

We are a remote-first organization, and we embrace an "accelerate from anywhere culture". You may be required to travel based on business requirements or for company/team events.

Responsibilities

  • Work with clients’ Medical Affairs and Scientific Communications teams to develop and execute strategic scientific communications initiatives such as scientific communications platforms, scientific communications plans, KOL engagement plans, etc.
  • Work with clients’ scientific teams to develop and execute both publications and medical communication tactics, such as manuscripts, abstracts, posters, review articles, symposia decks, literature searches, gap analyses, strategic publication plans, and MSL field materials.
  • Take ownership of client relationship by partnering with the Account Director to build confidence in company’s service offerings; ensure compliance and consistency with client SOPs, messaging, and scientific communications objectives; and assisting with resolution of client concerns.
  • Work with in-house technology and creative teams to build innovative digital solutions for Medical Affairs and Scientific Communications clients.
  • Oversee and be accountable for quality of scientific communications tactics/deliverables developed by in-house scientific writers. Review deliverables to ensure strategic alignment and scientific accuracy and be accountable for quality of deliverables sent to the client.
  • Develop, manage, and track strategy and tactics in partnership with a cross-functional team of internal and client stakeholders.
  • Train and mentor junior writers; contribute to skill development of the writing team.
  • Participate in client pitches and business development meetings as the scientific lead.
  • Ensure organic growth through ensuring quality deliverables and client engagement.

Qualifications And Prerequisites

  • MD, PhD, PharmD or similar advanced degree required.
  • At least 5 years of core writing experience and 3+ years of experience as a Medical Director at a pharmaceutical company or 7+ years of core writing experience and 2+ years as an Associate Medical Director.
  • Integrated Scientific Communications experience preferred with demonstrated experience on both medical communications and publications accounts.
  • Demonstrated expertise in developing and executing deliverables mentioned in the above for both investigational and mature products.
  • Experience across several therapy areas preferred.
  • Experience in writing/reviewing deliverables.
  • Experience with developing digital content and other deliverables to supplement traditional deliverables and communications.
  • Strong attention to detail and editorial skills needed.
  • Willingness to train and develop junior writers by doing detailed reviews of documents and training sessions.
  • Experience providing congress support and conducting/facilitating advisory board meetings a plus.
  • This role is fully remote (based anywhere in the US); travel to client locations, meetings, etc within the US and elsewhere will be required.
  • Must work East Coast times.

Benefits of this Role

  • Annual leaves, public holidays and a special day off for your birthday and work anniversary
  • Statutory leaves including SSP, maternity and paternity leaves
  • Comprehensive health coverage including eye tests.
  • Holistic wellness support with access to fitness club and sportive activites.
  • Financial security through life assurance and income protection
  • Retirement savings plan with employer contributions

Application Process

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. The selection process for this role includes an initial recruiter screening, an interview with the hiring manager, a strategic assessment, and HR interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

  • Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
  • Documenting work that brings everyone on the same page.
  • Maturity to choose between synchronous and asynchronous collaboration.
  • Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About CACTUS

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange - leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

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Divisional Medical Director

London, London Cygnet

Posted 17 days ago

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Job Description

Are you a dynamic and visionary clinical leader ready to shape the future of mental health care?


Are you ready to join an award-winning, industry-leading organisation where quality is at the heart of everything we do — and excellence is more than just a word, it's our culture? With just under 300 medical professionals on our team, we’re setting the standard for care.


Cygnet Health Care is seeking an exceptional Divisional Medical Director (DMD) to take on a pivotal executive leadership role. As the most senior medical leader within your division, you will drive the strategic direction, uphold the highest professional standards, and lead a high-performing medical workforce dedicated to delivering safe, effective, and person-centred care.

This is a unique opportunity to collaborate at the highest level across multidisciplinary teams, influence organisational priorities, and champion a culture of innovation, learning, and continuous improvement.


Cygnet distinguishes itself through a unique combination of scale, specialism, and personalisation of care. Our 13,000 staff support 8,300 individuals and with a portfolio of over 150 services, we offer care across a range of services from acute, PICU, Eating Disorders and CAMHS. We have a strong reputation for quality, inclusion, and staff satisfaction. We stand apart through our ability to deliver exceptional, high-acuity care at scale, underpinned by deep clinical understanding, sector-leading quality ratings, and an unwavering focus on person-centred practice.


We keep our focus on maintaining high-quality standards across all our services, consistently achieving sector-leading regulatory ratings across the UK. 81% of services evaluated earned a Good or Outstanding rating by regulators, outperforming the national average. Cygnet has 17% higher CQC Good or Outstanding ratings than the rest of the mental health independent sector and 95% of our hospitals are rated Good or Outstanding by our internal quality assessment team. Our collaboration with 360 commissioning bodies, has not only allowed us to support integrated pathways of care, but has also helped shape local and regional strategies for individuals with complex needs.


Cygnet has also been recognised externally, with recent wins at the HealthInvestor Awards including Specialist Care Provider of the Year and has also been recognised by the Carers Trust, with 20 of our services being awarded Triangle of Care accreditation.


Reporting directly to the Group Clinical Director, this is a full-time position responsible for strategic leadership of our Health Care South region (Including Greater London, South East, South West, South Wales and West Midlands). This is a remote role but will include travel to sites within this region 2 – 3 days per week, so access to a car & UK driving licence is essential.



Key Responsibilities:


Strategic and Clinical Leadership


  • Provide strategic clinical leadership across the division, setting high standards for medical practice and professional conduct.
  • Ensure alignment with national clinical policy and statutory requirements, championing evidence-based care, prevention, early intervention, and integrated models of service delivery.
  • Promote a strong culture of patient safety, learning, and openness in line with Just Culture principles.


Clinical Governance and Quality Improvement


  • Oversee clinical governance frameworks to ensure safe, effective, and person-centered care.
  • Lead on clinical quality improvement, audit, and innovation initiatives, ensuring high standards of care are maintained and continuously enhanced.
  • Promote adherence to policies relating to safeguarding, medicines optimisation, infection prevention and control, and controlled drug safety.


Medical Workforce Leadership


  • Lead on all aspects of clinical workforce planning, including recruitment, retention, role redesign, and succession planning.
  • Ensure a high-performing and appropriately skilled clinical workforce through oversight of appraisal, revalidation, CPD, and professional development.
  • Embed a culture of reflective practice, supervision, and 360-degree feedback within medical leadership.


Operational Excellence and Resource Stewardship


  • Work closely with the respective Managing Directors and regional clinical directors to ensure high-quality and high-value service delivery.
  • Ensure clinical productivity and resource utilisation are optimised, with clear outcome measures and benchmarking in place.
  • Contribute to the achievement of the overall financial targets by the division.


Innovation, Research and Partnership


  • Foster academic and clinical partnerships with external stakeholders, including NHS bodies, academic institutions, and research networks.
  • Promote engagement in ethically approved research, supporting a culture of inquiry, learning, and evidence-based practice.
  • Champion patient and resident involvement in research to inform service development and improve care outcomes.


We are looking for someone who is…


  • Extensively experienced in senior medical leadership, ideally at Associate Medical Director, Regional Medical Director, Divisional Director or equivalent level.
  • Holds an in-depth understanding of clinical and corporate governance frameworks.
  • Has comprehensive knowledge of the professional, educational, and regulatory requirements of the medical workforce.
  • Experienced in service redesign, workforce transformation and strategic planning.
  • Demonstrates a proven ability to lead change, manage complex teams and influence across organisational boundaries.
  • Demonstrates commitment to quality improvement and evidence-based practice in a multi-disciplinary setting.
  • Holds strong financial and budget management skills (desirable).
  • Experienced in medical research, audit, and clinical effectiveness.
  • Shows high emotional intelligence and excellent interpersonal skills, with the ability to navigate complexity and foster consensus.
  • Excellent written, verbal, and presentation skills, with the ability to engage diverse stakeholders.
  • Committed to ongoing personal and professional development, including the use of feedback tools such as MSF/360 appraisal.
  • Fully registered GMC & MBBS (or equivalent) qualified, and registered on the specialist register (CCT/CESR), Section 12 and AC Status


Why Cygnet? We’ll offer you…


  • Market leading salary and bonus
  • Company shares
  • Travel allowance
  • Generous annual leave entitlement that increases with length of service
  • Company paid Life Assurance scheme covering 3x salary
  • Contributory pension scheme
  • Electric Car Scheme
  • Free meals, on-site parking and EAP support
  • Research and teaching opportunities, as well as the opportunity to lead and participate in QI & Audit initiatives
  • A unique opportunity to lead the development of new services within the independent sector, shaping an innovative model of care from the ground up
  • Extensive development opportunities and monthly CPD groups
  • Peer‑led “Characters of Care” programme and a comprehensive employee benefit and support programme
  • 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
  • Smart Health Toolkit, including 24 hour GP service with the option of prescription delivery to your local pharmacy


If you would like to discuss this informally we’d be more than happy to facilitate this. Please contact: Hannah Dunlop via or 077 20 497 792


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.


*Recruitment agencies please note: Speculative emails are not to be sent directly to our clinical staff, these need to go via our internal recruitment team. If speculative candidates are sent directly to a member of the clinical team, we will consider these candidates as our own*

This advertiser has chosen not to accept applicants from your region.

Divisional Medical Director

Cygnet

Posted 17 days ago

Job Viewed

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Job Description

Are you a dynamic and visionary clinical leader ready to shape the future of mental health care?


Are you ready to join an award-winning, industry-leading organisation where quality is at the heart of everything we do — and excellence is more than just a word, it's our culture? With just under 300 medical professionals on our team, we’re setting the standard for care.


Cygnet Health Care is seeking an exceptional Divisional Medical Director (DMD) to take on a pivotal executive leadership role. As the most senior medical leader within your division, you will drive the strategic direction, uphold the highest professional standards, and lead a high-performing medical workforce dedicated to delivering safe, effective, and person-centred care.

This is a unique opportunity to collaborate at the highest level across multidisciplinary teams, influence organisational priorities, and champion a culture of innovation, learning, and continuous improvement.


Cygnet distinguishes itself through a unique combination of scale, specialism, and personalisation of care. Our 13,000 staff support 8,300 individuals and with a portfolio of over 150 services, we offer care across a range of services from acute, PICU, Eating Disorders and CAMHS. We have a strong reputation for quality, inclusion, and staff satisfaction. We stand apart through our ability to deliver exceptional, high-acuity care at scale, underpinned by deep clinical understanding, sector-leading quality ratings, and an unwavering focus on person-centred practice.


We keep our focus on maintaining high-quality standards across all our services, consistently achieving sector-leading regulatory ratings across the UK. 81% of services evaluated earned a Good or Outstanding rating by regulators, outperforming the national average. Cygnet has 17% higher CQC Good or Outstanding ratings than the rest of the mental health independent sector and 95% of our hospitals are rated Good or Outstanding by our internal quality assessment team. Our collaboration with 360 commissioning bodies, has not only allowed us to support integrated pathways of care, but has also helped shape local and regional strategies for individuals with complex needs.


Cygnet has also been recognised externally, with recent wins at the HealthInvestor Awards including Specialist Care Provider of the Year and has also been recognised by the Carers Trust, with 20 of our services being awarded Triangle of Care accreditation.


Reporting directly to the Group Clinical Director, this is a full-time position responsible for strategic leadership of our Health Care South region (Including Greater London, South East, South West, South Wales and West Midlands). This is a remote role but will include travel to sites within this region 2 – 3 days per week, so access to a car & UK driving licence is essential.



Key Responsibilities:


Strategic and Clinical Leadership


  • Provide strategic clinical leadership across the division, setting high standards for medical practice and professional conduct.
  • Ensure alignment with national clinical policy and statutory requirements, championing evidence-based care, prevention, early intervention, and integrated models of service delivery.
  • Promote a strong culture of patient safety, learning, and openness in line with Just Culture principles.


Clinical Governance and Quality Improvement


  • Oversee clinical governance frameworks to ensure safe, effective, and person-centered care.
  • Lead on clinical quality improvement, audit, and innovation initiatives, ensuring high standards of care are maintained and continuously enhanced.
  • Promote adherence to policies relating to safeguarding, medicines optimisation, infection prevention and control, and controlled drug safety.


Medical Workforce Leadership


  • Lead on all aspects of clinical workforce planning, including recruitment, retention, role redesign, and succession planning.
  • Ensure a high-performing and appropriately skilled clinical workforce through oversight of appraisal, revalidation, CPD, and professional development.
  • Embed a culture of reflective practice, supervision, and 360-degree feedback within medical leadership.


Operational Excellence and Resource Stewardship


  • Work closely with the respective Managing Directors and regional clinical directors to ensure high-quality and high-value service delivery.
  • Ensure clinical productivity and resource utilisation are optimised, with clear outcome measures and benchmarking in place.
  • Contribute to the achievement of the overall financial targets by the division.


Innovation, Research and Partnership


  • Foster academic and clinical partnerships with external stakeholders, including NHS bodies, academic institutions, and research networks.
  • Promote engagement in ethically approved research, supporting a culture of inquiry, learning, and evidence-based practice.
  • Champion patient and resident involvement in research to inform service development and improve care outcomes.


We are looking for someone who is…


  • Extensively experienced in senior medical leadership, ideally at Associate Medical Director, Regional Medical Director, Divisional Director or equivalent level.
  • Holds an in-depth understanding of clinical and corporate governance frameworks.
  • Has comprehensive knowledge of the professional, educational, and regulatory requirements of the medical workforce.
  • Experienced in service redesign, workforce transformation and strategic planning.
  • Demonstrates a proven ability to lead change, manage complex teams and influence across organisational boundaries.
  • Demonstrates commitment to quality improvement and evidence-based practice in a multi-disciplinary setting.
  • Holds strong financial and budget management skills (desirable).
  • Experienced in medical research, audit, and clinical effectiveness.
  • Shows high emotional intelligence and excellent interpersonal skills, with the ability to navigate complexity and foster consensus.
  • Excellent written, verbal, and presentation skills, with the ability to engage diverse stakeholders.
  • Committed to ongoing personal and professional development, including the use of feedback tools such as MSF/360 appraisal.
  • Fully registered GMC & MBBS (or equivalent) qualified, and registered on the specialist register (CCT/CESR), Section 12 and AC Status


Why Cygnet? We’ll offer you…


  • Market leading salary and bonus
  • Company shares
  • Travel allowance
  • Generous annual leave entitlement that increases with length of service
  • Company paid Life Assurance scheme covering 3x salary
  • Contributory pension scheme
  • Electric Car Scheme
  • Free meals, on-site parking and EAP support
  • Research and teaching opportunities, as well as the opportunity to lead and participate in QI & Audit initiatives
  • A unique opportunity to lead the development of new services within the independent sector, shaping an innovative model of care from the ground up
  • Extensive development opportunities and monthly CPD groups
  • Peer‑led “Characters of Care” programme and a comprehensive employee benefit and support programme
  • 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
  • Smart Health Toolkit, including 24 hour GP service with the option of prescription delivery to your local pharmacy


If you would like to discuss this informally we’d be more than happy to facilitate this. Please contact: Hannah Dunlop via or 077 20 497 792


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.


*Recruitment agencies please note: Speculative emails are not to be sent directly to our clinical staff, these need to go via our internal recruitment team. If speculative candidates are sent directly to a member of the clinical team, we will consider these candidates as our own*

This advertiser has chosen not to accept applicants from your region.

Medical Director Clinical Development

Cambridge, Eastern ARTO

Posted 1 day ago

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Job Description

ARTO have partnered with a highly funded biotechnology company with an innovative preclinical platform looking to find therapeutic candidates for diseases in Autoimmune, Neurological and Cardiovascular diseases.


As their research moves towards the clinic and phase I, we are now searching for a Medical Director to oversee the drafting of the IND packages, prepare for the company's drug development plan and also be a key member of the R&D team.


For this position, the ideal candidate would be based in the UK, with a bi-weekly office expectation of roughly 3 days in Cambridge.


Responsibilities:

  • Implement translational medicine and early clinical development plans for different therapeutic candidates
  • Prepare for Phase I clinical trials
  • Design and Implement clinical development plans
  • Lead the prep of regulatory submission documents.
  • Build relationships with stakeholders, senior management, KOLs


Qualifications:

  • MD, with experience working as a Clinical lead for early phase clinical trials.
  • Strong scientific background in Immunology/Inflammation/Dermatology and exposure and understanding of multiple disease areas and also drug development/discovery processes
  • Proven experience leading Phase I and II clinical trials.
  • At least 5 years of experience in industry from a pharmaceutical/biotech company.
  • Ability to work hands on in a dynamic team.


+447476557042

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Medical Director Clinical Development

Greater London, London ARTO

Posted 1 day ago

Job Viewed

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Job Description

ARTO is currently partnered with a globally renowned mid sized Pharmaceutical company who are committed to the development of drugs within the Rare Disease space.


With a growing clinical development team, we are currently searching for a Medical Director in their Clinical Development group who will be able to assist with the development of drugs from proof of concept up to the crucial NDA/BLA submission phase.


Key Responsibilities:

  • Medical Oversight : Acts as Medical Monitor, overseeing study execution, subject eligibility, and safety surveillance.
  • Scientific Leadership : Provides medical input on clinical study and protocol design, as well as driving clincial and project groups through execution
  • Data Analysis & Interpretation : Critically evaluates study data and contributes to the integration and interpretation of results.
  • Strategic Contribution : Supports the Clinical Development Plan (CDP) by aligning studies with broader clinical and scientific strategy.
  • Stakeholder Collaboration : Engages with internal teams and external physician stakeholders to inform clinical decisions and ensure relevance.


Experience Needed:

  • MD/MD PhD
  • 5 Years experience in the pharmaceutical industry
  • Experience as a Clinical Lead
  • Rare Disease experience preffered, but experience developing drugs in the wider Immunology space is also acceptable


If you'd like to hear more, please reach out to me on , or directly on LinkedIn DM!

This advertiser has chosen not to accept applicants from your region.

(Associate) Medical Director - Neurology

ThermoFisher Scientific

Posted 26 days ago

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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.
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Medical Director, Clinical Development - Hematology/Oncology

Uxbridge, London Gilead Sciences, Inc.

Posted 26 days ago

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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.
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(Senior) Medical Director - Rheumatology (Client - dedicated), EMEA

ThermoFisher Scientific

Posted 26 days ago

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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.
This advertiser has chosen not to accept applicants from your region.

Medical Director- Oncology / Directeur Mdical en Oncologie

GE HealthCare

Posted 26 days ago

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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
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