Thermo Fisher Scientific
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.
Senior Medical Director – Rheumatology, EMEA
🔥 2 hours ago
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship 2 hours ago
Thermo Fisher Scientific
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.
📋 Description
• Provide medical leadership to clinical study teams • Create clinical trial protocols using current scientific information • Contribute to site selection and review or approve study protocols and amendments, CSRs, ICFs, CRFs, protocol deviation decisions, and other clinical documents • Perform real-time medical monitoring of clinical studies • Ensure medical validity of primary endpoints and study subject safety • Identify medical issues early and proactively address customer concerns with the Global Medical Indication Lead • Consult internal groups on procedural and budgetary items and protocol amendments • Coordinate internal functions to close gaps and resolve issues • Serve as liaison between the sponsor and PPD internal departments throughout study phases • Educate investigator sites on protocol-specific laboratory procedures • Manage day-to-day clinical trial activities and resolve issues or answer queries • Act as medical point of contact for internal and external stakeholders • Interact with investigators and answer IRB and Health Authority questions • Prepare and present materials to study executives and independent safety committees • Provide medical training to site staff and CRA training for new indications • Ensure compliance with medical aspects of studies, SOPs, and GCP • Collaborate with cross-functional study teams to communicate medical risks, issues, and results
🎯 Requirements
• Medical Doctor, with a specialty in Rheumatology • Clinical experience treating patients in hospital • Significant experience within the pharmaceutical industry, clinical trials, and pharmaceutical medicine • Fluency in spoken and written English • Understanding and experience with NDA submission process • Understanding of regulatory guidelines for adverse event reporting • Strong communication and presentation skills • Strong teamwork skills • Ability to understand and apply relevant SOPs and GCP
🏖️ Benefits
• Global career development resources • Work with a global team of 100,000+ colleagues • EEO/Affirmative Action workplace • Meaningful work supporting life-changing therapies and improved health outcomes
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