Medical Director – Nephrology/Internal Medicine

🔥 15 hours ago

🌐 Italy, Serbia, +10 more countries – Remote

🇮🇹 Italy – Remote 🇷🇸 Serbia – Remote 🇩🇰 Denmark – Remote 🇷🇴 Romania – Remote 🇨🇿 Czechia – Remote 🇧🇬 Bulgaria – Remote 🇳🇱 Netherlands – Remote 🇭🇺 Hungary – Remote 🇵🇹 Portugal – Remote 🇧🇪 Belgium – Remote 🇪🇸 Spain – Remote 🇭🇷 Croatia – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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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 support and medical advice for clinical trials and safety evaluation within the client environment • Provide medical leadership to study teams • 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 • Ensure medical validity of primary endpoints and subject safety • Identify medical issues early and address customer concerns and corrective actions with the Global Medical Indication Lead • Consult internal groups on procedural and budgetary items and protocol amendments • Coordinate internal functions to close gaps and address issues • Liaise between the sponsor and PPD internal departments throughout study phases • Educate investigator sites through protocol-specific lab procedures presentations and demonstrations • Manage day-to-day clinical trial activities, resolve issues and answer queries • Serve 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 • Deliver 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 on medical risks, issues and results

🎯 Requirements

• Medical Doctor, with a specialty in Nephrology or Internal Medicine • Shown clinical experience running nephrology patients in hospital practice • Industry experience in clinical development required • Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine • Fluent in spoken and written English • Shown understanding and experience with NDA submission process • Shown understanding of regulatory guidelines for adverse event reporting • Strong communication & presentation skills • Strong teammate • Understanding and application of relevant SOPs and GCP

🏖️ Benefits

• Resources needed to achieve individual career goals • Diverse experiences, backgrounds and perspectives are valued • EEO/Affirmative Action protections • Standard Monday–Friday work schedule

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