
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
🕒 5 days ago
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship 5 days ago
Still open on Thermo Fisher Scientific's site. Checked 6 minutes ago.

10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
• Provide medical leadership to study teams and contribute to clinical trial protocols, site selection, protocol and amendment review, CSRs, ICFs, CRFs, protocol deviation decisions and other clinical documents • Perform real-time medical monitoring of clinical studies, ensuring endpoint validity, subject safety and early identification of medical issues • Address customer concerns and correct issues in consultation 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 sponsors and internal departments throughout study phases • Educate investigator sites on protocol-specific laboratory procedures • Manage day-to-day clinical trial activities, resolve issues and answer queries • Act as 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 • Provide medical training to site staff and CRA training in new indications • Ensure medical compliance with relevant SOPs and GCP • Collaborate with cross-functional study teams to communicate medical risks, issues and results
• MD, MB/BS or equivalent degree • Strong medical knowledge • Clinical experience running Neurology patients in hospital practice • 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 • Epileptology experience is advantageous
• EEO/Affirmative Action Employer • Mission-driven work contributing to healthier, cleaner and safer outcomes • Resources to achieve individual career goals • Diverse and inclusive workplace where diverse experiences, backgrounds and perspectives are valued
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🕒 October 8
Medical Director guiding safety evaluation, benefit-risk assessment, and pharmacovigilance for a global pharmaceutical company. Remote from Portugal on a one-year contract with potential extension.