Director Medical Device jobs in Oxford
- ICON PlcReading
- Providing strategic medical leadership and guidance on project teams.
- Offering expert medical and scientific consultation throughout project lifecycles.
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- Vertex PharmaceuticalsOxford
- Using deep scientific expertise and strong leadership skills, this role will provide strategic and scientific direction to help advance the discovery and…
- Novo NordiskOxford
- You are an experienced pharmaceutical Ethics & Compliance professional who can combine regulatory expertise with sound judgement, pragmatism and a strong…
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- University of OxfordOxford
- You will lead major gift fundraising for one of Oxford’s highest performance teams and build meaningful donor relationships to help shape the future of medical…
- Sarepta TherapeuticsReading
- Experience generating and communicating actionable medical insights that influence strategy and decision making.
- Significant experience in medical safety, pharmacovigilance, or medical monitoring within the pharmaceutical, biotechnology, CRO, or healthcare industry.
- View all IQVIA jobs - Reading jobs - Safety Director jobs in Reading
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- ReplimuneAbingdon
- The Qualified Person (QP) must fulfil duties in compliance with Eudralex Volume 4, Annex 16, Certification by a Qualified Person and Batch Release.
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- ImmunocoreOxford
- Provide operational and leadership continuity across Immunocore's medicinal product lifecycle by deputizing for the Director, Quality Assurance, and supporting…
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- Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
- University of OxfordOxford
- A medical degree and/or PhD in a relevant medical research field.
- Through strong partnerships across Indonesia and the wider region, OUCRU-IND is committed to…
- CBRE Scientific Solutions is seeking a Business Development Director to drive growth across our Life Sciences, Pharmaceutical, Biotech and Advanced…
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- ICON PlcReading
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Your experience in Observational Research, Real-World Evidence,…
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- Based within the Clinical Pharmacology group in Moderna’s Clinical and Quantitative Pharmacology (CQP) function, you will bring deep technical, quantitative,…
- ReplimuneAbingdon
- The Associate Director - Process Development is responsible for managing the Process Development team at Replimune’ s Milton Park facility.
- ReplimuneAbingdon
- The Associate Director - Process Development is responsible for managing the Process Development team at Replimune’ s Milton Park facility.
- OrganOxOxford
- This role requires a highly experienced programme leader with a proven track record of delivering complex medical device development programmes within regulated…
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Job Post Details
Medical Director
Job details
Full job description
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Medical Director at ICON, you will drive medical initiatives within project teams, guiding strategic direction and decision-making processes, and offer expert medical and scientific guidance, leveraging therapeutic expertise to inform project development.
What You Will Do:
You will lead medical affairs delivery across your portfolio, setting standards and developing your team.
Key responsibilities include:
- Medical Director will support multiple studies; however, the scope will be focused primarily on site support activities , including responding to site questions and reviewing laboratory results.
- Providing strategic medical leadership and guidance on project teams.
- Offering expert medical and scientific consultation throughout project lifecycles.
- Ensuring compliance with ethical, legal, and regulatory standards in medical and safety monitoring activities.
- Representing the Medical Affairs Department in business development initiatives.
- Providing operational oversight within the Medical Affairs Department as needed.
Your Profile:
You will bring significant medical monitoring and clinical oversight experience, with demonstrated expertise in managing clinical site queries and reviewing/escalating critical laboratory alerts.
Required qualifications and experience:
- Medical degree (MD) or equivalent qualification - Cardiology MD OR Endocrinology/Diabetes/Obesity or Internal Medicine MDs
- Cardiovascular Outcomes trial experience or obesity/ GLP1 experience is a must for the role
- Extensive experience in clinical research and development,
- Strong understanding of clinical trial design, regulatory requirements, and GCP guidelines.
- Exceptional analytical and problem-solving skills, with a focus on interpreting clinical data and driving evidence-based decisions.
- Excellent leadership, communication, and collaboration skills, with the ability to work effectively in cross-functional, global teams.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request .
Are you a current ICON Employee?