14 Clinical Oncology jobs in the United Kingdom
Clinical Oncology Consultant
Posted 66 days ago
Job Viewed
Job Description
Contact
Experience Required: NHS experience essential
We are seeking an experienced and dedicated Clinical Oncology Consultant to join a leading healthcare provider in Derby . This permanent role offers an excellent opportunity to contribute to a dynamic oncology team, providing high-quality cancer care within an NHS setting.
Key Responsibilities:- Provide specialist clinical oncology services, including chemotherapy and radiotherapy treatment planning.
- Lead and support multidisciplinary team meetings, collaborating with oncologists, radiologists, surgeons, and other healthcare professionals.
- Develop and implement patient treatment plans, ensuring the highest standards of care and patient safety.
- Supervise and train junior doctors, nurses, and other healthcare staff.
- Participate in research, audits, and quality improvement initiatives within the department.
- Maintain up-to-date knowledge of advancements in oncology treatments and best practices.
- Engage in teaching activities for medical students and junior staff.
- Contribute to service development and clinical governance within the department.
Requirements
Full GMC registration with a license to practice.
CCT (Certificate of Completion of Training) in Clinical Oncology or eligibility within six months.
Extensive NHS experience in oncology.
Strong leadership, communication, and team-working skills.
Experience in chemotherapy, radiotherapy planning, and multidisciplinary team collaboration.
Benefits
- Competitive salary and NHS benefits package.
- Opportunities for professional development and research.
- Supportive and well-established oncology department.
- Access to state-of-the-art treatment facilities and cutting-edge technology.
If you are an experienced Clinical Oncology Consultant looking for a new opportunity in Derby , we would love to hear from you.
Medical Director, Clinical Development - Hematology/Oncology
Posted 5 days ago
Job Viewed
Job Description
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.
Bank Oncology / Chemotherapy Nurse
Posted 14 days ago
Job Viewed
Job Description
Bank Oncology Nurse | Oadby, Leicester | Competitive rates, plus enhancements | Bank contract | No nights | Monday - Friday, 8am-6pm |
Due to our oncology service increasing, Spire Leicester Hospital are looking for experienced oncology nurses to join our team of bank nurses on our 17 bedded, purpose-built, dedicated oncology and haematology unit.
Working alongside a team of 12 Nurses, 1 HCA and several consultants, you will receive a huge level of support from your team members.
We promote a good work/life balance and to support this you will work no nights or weekends and very rare bank holidays.
Founded in 1989, Spire Leicester is a high performing hospital with a great track record in superior patient care. We practice some of the most advanced treatments on the latest generation imaging, and diagnostic technology, meaning we can offer everything from screening, rehabilitation and cutting-edge surgical procedures in specialist fields like orthopaedics and cancer care.
Duties and responsibilities:
To provide safe administration of Systemic Anti-Cancer Therapy, specialist nursing care of central lines, assist in oncology clinics, provide advice and support to oncology and haematology patients and their family members. The service provided will primarily be for the daycare oncology unit and outpatients but you may also be required to support the care of patients admitted to the ward from the unit.
What are we looking for?
- Current oncology experience
- NMC Registered Nurse, with no restrictions
- A positive attitude and team player
- Strong communication skills
- Cannulation and venepuncture trained
- You must be SACT administration trained
Benefits
We offer employees a competitive salary as well as a comprehensive benefits package which includes but is not limited to:
- 35 days annual leave inclusive of bank holidays
- Employer and employee contributory pension with flexible retirement options
- 'Spire for you' reward platform - discount and cashback for over 1000 retailers
- Free Bupa wellness screening
- Private medical insurance
- Life assurance
- Free onsite parking
Please see the attached benefits leaflet for more information.
We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.
For further information about this role or for an informal conversation about the range of career options available with Spire please contact Hananh Radford on
For us, it's more than just treating patients; it's about looking after people.
Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications
Bank Oncology / Chemotherapy Nurse
Posted 1 day ago
Job Viewed
Job Description
Bank Oncology Nurse | Oadby, Leicester | Competitive rates, plus enhancements | Bank contract | No nights | Monday - Friday, 8am-6pm |
Due to our oncology service increasing, Spire Leicester Hospital are looking for experienced oncology nurses to join our team of bank nurses on our 17 bedded, purpose-built, dedicated oncology and haematology unit.
Working alongside a team of 12 Nurses, 1 HCA and several consultants, you will receive a huge level of support from your team members.
We promote a good work/life balance and to support this you will work no nights or weekends and very rare bank holidays.
Founded in 1989, Spire Leicester is a high performing hospital with a great track record in superior patient care. We practice some of the most advanced treatments on the latest generation imaging, and diagnostic technology, meaning we can offer everything from screening, rehabilitation and cutting-edge surgical procedures in specialist fields like orthopaedics and cancer care.
Duties and responsibilities:
To provide safe administration of Systemic Anti-Cancer Therapy, specialist nursing care of central lines, assist in oncology clinics, provide advice and support to oncology and haematology patients and their family members. The service provided will primarily be for the daycare oncology unit and outpatients but you may also be required to support the care of patients admitted to the ward from the unit.
What are we looking for?
- Current oncology experience
- NMC Registered Nurse, with no restrictions
- A positive attitude and team player
- Strong communication skills
- Cannulation and venepuncture trained
- You must be SACT administration trained
Benefits
We offer employees a competitive salary as well as a comprehensive benefits package which includes but is not limited to:
- 35 days annual leave inclusive of bank holidays
- Employer and employee contributory pension with flexible retirement options
- 'Spire for you' reward platform - discount and cashback for over 1000 retailers
- Free Bupa wellness screening
- Private medical insurance
- Life assurance
- Free onsite parking
Please see the attached benefits leaflet for more information.
We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.
For further information about this role or for an informal conversation about the range of career options available with Spire please contact Hananh Radford on
For us, it's more than just treating patients; it's about looking after people.
Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications
Oncology Specialist Nurse - Team Leader
Posted 14 days ago
Job Viewed
Job Description
Oncology Specialist Nurse | Team Leader | Full Time | Fixed Term Contract - 12 months | Leeds - LS8
We have an exciting opportunity for an experienced Chemotherapy Specialist Nurse Team Leader to join our Oncology team on full time, fixed term contract for 12 months.
- Shift Patterns: x4 shifts 08.00 - 18.00 - Monday-Friday
- 1 in 6 UKONS telephone triage on call from home
As the Oncology & Haematology Team leader, you are responsible for delivering nursing services to patients within the unit and to deputise for the cancer service lead. You will line manage a team of 5 chemotherapy nurses and 2 cancer service administrators.
Spire Leeds Hospital, located in Roundhay, Leeds, has been treating patients for almost 30 years. We are the region's largest private hospital in terms of the range of services we offer and the number of consultants we work with. The hospital offers a range of services and facilities including four operating theatres, a sterile services department, a dedicated endoscopy suite, and a diagnostic and imaging department with an MRI and CT scanner. There are outpatient and physiotherapy departments providing services six days per week
Duties and responsibilities
- Take responsibility for competency assessment of members of staff being line managed by you.
- Regular appraisals and 1:1s with those being line managed by you.
- Attending regular meetings on behalf of the cancer service lead.
- Ensuring safe staffing levels and managing rosters for team.
- Managing employee absence, including sickness, annual leave and other leave in line with absence policy in addition to managing employee behaviour in line with code of conduct.
- Participate in clinical audit within the chemotherapy service, raising the profile and enhancing the contribution of nursing to patient care and informing business and service development plans.
- To act as nurse in charge on shift and coordinate, providing clinical and managerial leadership to nursing and administration team.
- To respond to any reported incidents via DCIQ system and share learning with the team from these.
- Provide specialist nursing advice and support to patients, their families and other healthcare professionals following diagnosis and through all stages of treatment.
- Ensure continuity of a high standard of evidence-based nursing care for patients undergoing SACT.
- Use advanced history taking and assessment skills to assess health, health related and nursing needs of patients, taking into consideration the needs of their families and carers. Identify and initiate appropriate steps for effective care.
- Manage a patient caseload, ensuring patients' holistic needs are met and continually re-evaluated, as necessitated by changes in their health/health deterioration.
- Work autonomously whilst providing clinical leadership, ensuring all patients have an accurate plan of care, which reflects the assessment undertaken and incorporates the issues and recommendations made ensuring clear documentation in the patient's records.
- Use advanced communication skills to explore patients' complex issues, thoughts and feelings, and refer to specialist supportive services as necessary.
- Ensure smooth patient pathway by liaising with external health and support teams as required eg community palliative care, GPs, DNs, hospital AOS, dieticians, medical secretaries etc
- Triage unwell SACT patients using UKONS triage assessment tool, advise re symptoms/prescribe medication, arrange investigations or hospital admission - in accordance with consultant advice.
- Provide out-of-hours support and triage for patients who develop acute treatment complications.
- Work alongside radiographers, outpatient staff and chemotherapy staff to ensure holistic care is maintained throughout Spire Healthcare Leeds Hospital.
- Demonstrate advanced knowledge and skills in intravenous access, the management of central venous catheters, venepuncture, and chemotherapy delivery, including the management of anaphylaxis and extravasation.
- Practice intermediate life support to facilitate rapid stabilisation and the appropriate ongoing management of patients who develop treatment complications.
- Ensure all patients are fully informed of the risks and benefits of proposed procedures/treatments, contributing to the process of informed consent.
- Produce and provide all patients with relevant and accessible written information regarding their treatment, procedures and illness.
- Ensure all care is given in accordance with agreed protocols.
- Work in line with and contribute to local delivery of national care standards.
- Supervise and participate in the delivery of programmes of education and training per the identified needs of clients, carers and others involved in their care.
- Work with junior staff to identify knowledge gaps in relation to SACT patients and ensure staff are appropriately educated.
Who we're looking for
- Registered nurse with a valid NMC Pin - essential
- Hold a relevant degree or equivalent - essential
- Evidence of post-registration professional development - essential
- Have undertaken an advanced communications course - essential
- Have undertaken advanced history taking and assessment course - desirable
- Have undertaken chemotherapy course - essential
- Team player - essential
- Excellent communication and organisational skills - essential
- Relevant clinical experience working with oncology services - essential
- Evidence of service development/improvements to current services
- Flexibility to meet the needs of the service (eg flexible working hours) - essential
- Ability to work accurately and reliably under pressure
- Ability to make decisions, organise and prioritise
- Evidence of commitment to customer care initiatives
- Knowledge and understanding of quality issues
Benefits
We offer employees a competitive salary as well as a comprehensive benefits package which includes but is not limited to:
- 35 days annual leave inclusive of bank holidays
- Employer and employee contributory pension with flexible retirement options
- Spire for you' reward platform - discount and cashback for over 1000 retailers
- Free Bupa wellness screening
- Private medical insurance
- Life assurance
- Free onsite parking
Our Values
We are extremely proud of our heritage in private healthcare and of our values as an organisation:
- Driving clinical excellence
- Doing the right thing
- Caring is our passion
- Keeping it simple
- Delivering on our promises
- Succeeding and celebrating together
- Our people are our difference; it's their dedication, warmth and pursuit of excellence that sets Spire Healthcare apart.
For us, it's more than just treating patients; it's about looking after people
We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.
Spire Healthcare are proud to be an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive culture for all. Our people are our difference, it's their dedication, warmth and pursuit of excellence that sets Spire Healthcare apart.
For further information about this role or for an informal conversation about the range of career options available with Spire please contact Lauren Armitage on
Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications
Oncology Specialist Nurse - Team Leader
Posted 1 day ago
Job Viewed
Job Description
Oncology Specialist Nurse | Team Leader | Full Time | Fixed Term Contract - 12 months | Leeds - LS8
We have an exciting opportunity for an experienced Chemotherapy Specialist Nurse Team Leader to join our Oncology team on full time, fixed term contract for 12 months.
- Shift Patterns: x4 shifts 08.00 - 18.00 - Monday-Friday
- 1 in 6 UKONS telephone triage on call from home
As the Oncology & Haematology Team leader, you are responsible for delivering nursing services to patients within the unit and to deputise for the cancer service lead. You will line manage a team of 5 chemotherapy nurses and 2 cancer service administrators.
Spire Leeds Hospital, located in Roundhay, Leeds, has been treating patients for almost 30 years. We are the region's largest private hospital in terms of the range of services we offer and the number of consultants we work with. The hospital offers a range of services and facilities including four operating theatres, a sterile services department, a dedicated endoscopy suite, and a diagnostic and imaging department with an MRI and CT scanner. There are outpatient and physiotherapy departments providing services six days per week
Duties and responsibilities
- Take responsibility for competency assessment of members of staff being line managed by you.
- Regular appraisals and 1:1s with those being line managed by you.
- Attending regular meetings on behalf of the cancer service lead.
- Ensuring safe staffing levels and managing rosters for team.
- Managing employee absence, including sickness, annual leave and other leave in line with absence policy in addition to managing employee behaviour in line with code of conduct.
- Participate in clinical audit within the chemotherapy service, raising the profile and enhancing the contribution of nursing to patient care and informing business and service development plans.
- To act as nurse in charge on shift and coordinate, providing clinical and managerial leadership to nursing and administration team.
- To respond to any reported incidents via DCIQ system and share learning with the team from these.
- Provide specialist nursing advice and support to patients, their families and other healthcare professionals following diagnosis and through all stages of treatment.
- Ensure continuity of a high standard of evidence-based nursing care for patients undergoing SACT.
- Use advanced history taking and assessment skills to assess health, health related and nursing needs of patients, taking into consideration the needs of their families and carers. Identify and initiate appropriate steps for effective care.
- Manage a patient caseload, ensuring patients' holistic needs are met and continually re-evaluated, as necessitated by changes in their health/health deterioration.
- Work autonomously whilst providing clinical leadership, ensuring all patients have an accurate plan of care, which reflects the assessment undertaken and incorporates the issues and recommendations made ensuring clear documentation in the patient's records.
- Use advanced communication skills to explore patients' complex issues, thoughts and feelings, and refer to specialist supportive services as necessary.
- Ensure smooth patient pathway by liaising with external health and support teams as required eg community palliative care, GPs, DNs, hospital AOS, dieticians, medical secretaries etc
- Triage unwell SACT patients using UKONS triage assessment tool, advise re symptoms/prescribe medication, arrange investigations or hospital admission - in accordance with consultant advice.
- Provide out-of-hours support and triage for patients who develop acute treatment complications.
- Work alongside radiographers, outpatient staff and chemotherapy staff to ensure holistic care is maintained throughout Spire Healthcare Leeds Hospital.
- Demonstrate advanced knowledge and skills in intravenous access, the management of central venous catheters, venepuncture, and chemotherapy delivery, including the management of anaphylaxis and extravasation.
- Practice intermediate life support to facilitate rapid stabilisation and the appropriate ongoing management of patients who develop treatment complications.
- Ensure all patients are fully informed of the risks and benefits of proposed procedures/treatments, contributing to the process of informed consent.
- Produce and provide all patients with relevant and accessible written information regarding their treatment, procedures and illness.
- Ensure all care is given in accordance with agreed protocols.
- Work in line with and contribute to local delivery of national care standards.
- Supervise and participate in the delivery of programmes of education and training per the identified needs of clients, carers and others involved in their care.
- Work with junior staff to identify knowledge gaps in relation to SACT patients and ensure staff are appropriately educated.
Who we're looking for
- Registered nurse with a valid NMC Pin - essential
- Hold a relevant degree or equivalent - essential
- Evidence of post-registration professional development - essential
- Have undertaken an advanced communications course - essential
- Have undertaken advanced history taking and assessment course - desirable
- Have undertaken chemotherapy course - essential
- Team player - essential
- Excellent communication and organisational skills - essential
- Relevant clinical experience working with oncology services - essential
- Evidence of service development/improvements to current services
- Flexibility to meet the needs of the service (eg flexible working hours) - essential
- Ability to work accurately and reliably under pressure
- Ability to make decisions, organise and prioritise
- Evidence of commitment to customer care initiatives
- Knowledge and understanding of quality issues
Benefits
We offer employees a competitive salary as well as a comprehensive benefits package which includes but is not limited to:
- 35 days annual leave inclusive of bank holidays
- Employer and employee contributory pension with flexible retirement options
- Spire for you' reward platform - discount and cashback for over 1000 retailers
- Free Bupa wellness screening
- Private medical insurance
- Life assurance
- Free onsite parking
Our Values
We are extremely proud of our heritage in private healthcare and of our values as an organisation:
- Driving clinical excellence
- Doing the right thing
- Caring is our passion
- Keeping it simple
- Delivering on our promises
- Succeeding and celebrating together
- Our people are our difference; it's their dedication, warmth and pursuit of excellence that sets Spire Healthcare apart.
For us, it's more than just treating patients; it's about looking after people
We commit to our employees well-being through work life balance, on-going development, support and reward.
Spire Healthcare is a leading independent hospital group in the United Kingdom and the largest in terms of revenue. From 39 hospitals and 8 clinics across England, Wales and Scotland, Spire Healthcare provides diagnostics, inpatient, day case and outpatient care.
Spire Healthcare are proud to be an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive culture for all. Our people are our difference, it's their dedication, warmth and pursuit of excellence that sets Spire Healthcare apart.
For further information about this role or for an informal conversation about the range of career options available with Spire please contact Lauren Armitage on
Closing date: In order to streamline our recruitment process, we reserve the right to expire vacancies prior to the advertised closing date once we have received a sufficient number of applications
Senior Clinical Research Associate (Oncology Experience Required) - Midlands, UK (Remote) - FSP
Posted today
Job Viewed
Job Description
Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.
Our CRAs work from their home office base, supporting studies within their country or region. 'Manageable sites, manageable protocols' is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
**Some specifics about this advertised role**
+ Dedicated to one client.
+ Responsible for all site management and monitoring activities across assigned oncology studies
+ Work with industry leaders and subject matter experts.
+ Opportunity to mentor junior CRAs.
+ Work with world-class technology.
+ a pivotal role in the drug development process.
**Here are a few requirements specific to this advertised role.**
+ Substantial Site Management experience, with an understanding of the clinical
+ trial methodology and terminology.
+ Experience in, or willingness to monitor oncology clinical trials.
+ Experience in independent monitoring, all types of visits.
+ Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
+ Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
**Who are Parexel**
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You'll be an influential member of the wider team.
**Not quite the role for you?**
Join Our Talent Community and we'll reach out with job alerts when positions that match your career interests become available. We'll also share periodic updates about the latest company news and events.
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Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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Medical Director- Oncology / Directeur Mdical en Oncologie
Posted 5 days ago
Job Viewed
Job Description
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
Medical Director- Oncology / Directeur Mdical en Oncologie
Posted 5 days ago
Job Viewed
Job Description
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
Medical Director - Oncology/Hematology , Home- Based (m/w/d)
Posted 3 days ago
Job Viewed
Job Description
The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs.
The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues, and to provide review of alert labs per sponsor preference. Major duties of the Medical Director are outlined below:
**Essential Functions**
Functions as project team member:
+ Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting.
+ Ensures medical activities run according to GCP and operate with highest efficiency.
+ Establishes and maintains a network of medical/scientific consultants, etc.
+ Supervises and manages Medical Director activities.
Clinical Activities:
+ Interacts with clients regarding drug development programs, study design and protocol.
+ Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
+ Interacts in team approach to develop statistical and data management sections of the protocol.
+ Reviews the final protocol for clinical, safety and efficacy variables.
+ Provides project team training on protocol and/or therapeutic areas.
+ Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
+ Participates in subject recruitment and retention activities including individual calls to key opinion leaders, investigators, and site staff and/or participation in teleconference and WebEx presentations.
+ Presents protocol and/or safety reporting information at investigator meetings.
+ Develops project medical monitoring plans as requested.
+ Provides on call coverage for protocol queries and site support.
+ Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
Safety Monitoring and SAE Reporting Activities:
+ Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
+ Provides medical review of SAE reporting, writes and/or reviews SAE narratives, and works with the Safety Management Department to track SAEs and follow-up on outstanding safety queries, interacts with sponsor and discusses safety issues with site as needed.
+ Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.
+ In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).
+ Interact with appropriate FDA officials concerning safety and other study related issues, as requested.
Data Activities:
+ Provides medical review of eCRFs for clinical accuracy.
+ Provides medical review of data analysis plan.
+ Reviews safety fields at case freeze for reconciliation (if needed).
+ Works with data group to reconcile SAE events as needed.
+ Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.
+ Reviews data tables, listings, and figures.
+ Reviews and/or writes portions of final clinical study report.
DSMB/Adjudication Committee Activities:
+ May assist sponsor in choosing committee members.
+ May serve as a non-voting member to convene and organize proceedings.
+ May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.
+ May determine data flow with sponsor to ensure reporting accuracy.
+ Can ensure DSMB feedback is given to sites for IRBs.
+ All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.
Business Development Activities:
+ Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.
+ Supports business development activities with proposal development and sales presentations.
+ Participates in feasibility discussions relating to specific project proposals.
Special Projects:
+ Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
+ Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.
+ Participate in a variety of team quality improvement efforts as necessary.
+ Perform other related duties as assigned or requested by the Chief Medical Officer.
**Qualifications**
+ Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
+ 10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.
+ 3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.
+ Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
+ Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
+ Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
+ Excellent oral and written communications skills as well as interpersonal skills are essential.
**Oncology / Hematology**
+ Current or prior license to practice medicine; board certification/eligibility ideal (Preference)
+ Board Certified / Board Eligible: Oncology/ Hematology (Required)
**Applicants must have experience in at least one of the following areas: Hematology (Non-Malignant) , Hematological Malignancies ,Solid Tumor Oncology , Radiation Oncology / Radiation Therapy , Pediatric Hematology / Oncology , Histopathology / Pathology , Gynecology or Urology.**
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 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.
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