Clinical Trial Physician – Phase I, EMEA

🔥 1 minute ago

🇧🇪 Belgium – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 10%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

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 study teams • Create clinical trial protocols using the latest scientific information • Contribute to site selection and review and approval of 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 • Proactively escalate and correct medical issues in consultation with the Global Medical Indication Lead • Interpret clinical trial data for regulatory documents, manuscripts, and other publications • Act as medical point of contact for internal and external stakeholders • Interact with investigators and answer questions from IRBs and Health Authorities • Prepare and present material 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 team members to clarify medical risks, issues, and results • Harmonize answers, eligibility decisions, and protocol deviation decisions when multiple physicians work on a protocol

🎯 Requirements

• Medical Doctor • Relevant specialty education preferred, such as neurology, hematology, dermatology, immunology, rheumatology, internal medicine, or pediatrics • Some experience in industry preferred • Excellent English, written and spoken • Ability to travel • Proven interpersonal skills to lead a study team and provide medical advice and evaluations • Proactive problem-solving and negotiation skills • Strong communication skills for collaboration in a cross-functional, matrix structure • Knowledge and application of relevant SOPs and GCP • Ability to exercise judgment and escalate issues immediately when needed

🏖️ Benefits

• Healthy and balanced work environment • Collaboration and professional development opportunities • Ability to travel

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