Clinical Trial Physician – Phase I, EMEA

Job not on LinkedIn

🔥 19 hours ago

🌐 Belgium, Denmark, +4 more countries – Remote

🇧🇪 Belgium – Remote 🇩🇰 Denmark – Remote 🇵🇹 Portugal – Remote 🇷🇸 Serbia – Remote 🇳🇱 Netherlands – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

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.

📋 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 • Review Clinical Study Reports, Informed Consent Forms, Case Report Forms, protocol deviation decisions, and other clinical documents • Conduct real-time medical monitoring of clinical studies • Ensure medical validity of primary endpoints and study subject safety • Identify, 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 IRB and Health Authority questions • 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 study compliance for medical aspects by applying SOPs and GCP • Collaborate with cross-functional study team members on medical risks, issues, and results • Harmonize site/IRB/RA 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 • Sensitivity to different cultural needs in a global organization • Strong communication and collaboration skills • Ability to gather decision information, negotiate, and communicate decisions and actions • Understanding and application of relevant SOPs and GCP

🏖️ Benefits

• Healthy and balanced work environment • Collaboration and development opportunities • Ability to work as part of a global team • Meaningful work contributing to life-changing therapies and improved health outcomes

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