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(Associate) Medical Director - Dermatology, Emea - (A-075)

Detalles de la oferta

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
Please do not contact the recruiter directly.
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 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.
Discover Impactful Work: The Dermatologist Medical Director provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators, and project team members, and supports business development activities.
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 through feasibility support, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), protocol deviation decisions, and other documents requiring medical input. Ensure medical validity of each individual primary endpoint as well as 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. Serve as chief medical liaison between sponsor and all PPD internal departments performing the required tasks during all study phases. Liaise with Investigator sites by delivering protocol-specific advice on subject eligibility, protocol clarifications, and safety concerns.
Medical Monitoring of clinical studies: Medical point of contact for all internal and external stakeholders. Interacts with the investigators as needed, answers questions of IRBs and Health Authorities, prepares and presents 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 collaborates with the cross-functional study team members for medical risks, issues, and results to be clear to all involved parties.
Education: MD degree or equivalent board certified in Dermatology. Active medical licensure (preferably in country of residence). 4+ years relevant experience such as pharmaceutical industry or CRO, in clinical development or pharmacovigilance or significant clinical trial experience as a principal investigator. 5+ years medical experience as a Dermatologist treating physician. Previous experience with cell-therapy or gene therapy.
Knowledge, Skills, Abilities: Experience within pharmaceutical industry, clinical trials, and pharmaceutical medicine is considered beneficial. Fluent in spoken and written English. Strong communication & presentation skills. A team player.
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!
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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Salario Nominal: A convenir

Fuente: Jobleads

Requisitos

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