Medical Director – Nephrology, Internal Medicine

🔥 2 minutes ago

🇷🇸 Serbia – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 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 clinical study teams • Create clinical trial protocols using the latest scientific information • Contribute to site selection and review and approve study protocols and 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 participant safety • Identify medical issues early and proactively address customer concerns and corrections with the Global Medical Indication Lead • Consult internal groups and support staff on procedural and budgetary items and protocol amendments • Coordinate functions to close gaps and address issues timely and effectively • Serve as chief liaison between the sponsor and PPD internal departments throughout all study phases • Educate investigator sites through protocol-specific laboratory procedures presentations and demonstrations • Manage day-to-day clinical trial activities, resolve issues, and answer queries • 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 materials to study executives and independent safety committees when applicable • Provide medical training to site staff and CRA training in new indications • Ensure compliance with relevant SOPs and GCP • Collaborate with cross-functional study team members to clarify medical risks, issues, and results

🎯 Requirements

• Medical Doctor with a specialty in Nephrology or Internal Medicine • Clinical experience treating nephrology patients in hospital practice • Industry experience in clinical development • Significant experience within the pharmaceutical industry, clinical trials, and pharmaceutical medicine • Fluent 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

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Equal employment opportunity and affirmative action environment • Diverse, inclusive workplace where diverse experiences, backgrounds, and perspectives are valued

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