
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
Biotechnology • Pharmaceuticals • Healthcare
Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.
🔥 3 minutes ago
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship 3 minutes ago

10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
Biotechnology • Pharmaceuticals • Healthcare
Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.
• Provide medical leadership to study teams for Dermatology clinical trials and safety evaluation within the PPD Pharmacovigilance department • Create clinical trial protocols using the latest scientific information • Contribute to site selection and review and approve study protocols, amendments, CSRs, ICFs, CRFs, protocol deviation decisions, and other clinical documents • Conduct real-time medical monitoring of clinical studies and ensure endpoint validity and subject safety • Identify medical issues early and address customer concerns in consultation with the Global Medical Indication Lead • Consult internal groups on procedural and budgetary items and protocol amendments • Coordinate internal departments and liaise between the sponsor and PPD departments throughout study phases • Educate investigator sites through protocol-specific lab procedure presentations and demonstrations • Manage day-to-day clinical trial activities, resolve issues, and answer queries • Act as the medical point of contact for internal and external stakeholders, investigators, IRBs, and Health Authorities • Prepare and present materials to study executives and independent safety committees when applicable • Provide medical training to site staff and CRA training in new indications • Ensure compliance with medical aspects of studies by applying relevant SOPs and GCP • Collaborate with cross-functional study teams to communicate medical risks, issues, and results
• Medical Doctor with a specialty in Dermatology, Allergology, Immunology, or Rheumatology • 2+ years of experience within the pharmaceutical industry, clinical trials, and pharmaceutical medicine • Previous experience in a hospital setting • Fluency in spoken and written English • Understanding and experience with the NDA submission process • Understanding of regulatory guidelines for adverse event reporting • Strong communication and presentation skills • Strong teamwork skills • Understanding and application of relevant SOPs and GCP
• Global company resources to support individual career goals • Meaningful work contributing to healthier, cleaner and safer outcomes • Diverse and inclusive workplace valuing varied experiences, backgrounds and perspectives • EEO/Affirmative Action protections • Opportunity to work with clinical research, digital and decentralized clinical trial services
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