Medical Director – Pulmonology

🔥 12 minutes ago

🇷🇸 Serbia – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 15%

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

🧬 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 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 study subject safety • Identify medical issues early and proactively address customer concerns and corrective actions • Consult internal groups regarding procedural and budgetary items and protocol amendments • Coordinate with functions to close gaps and address issues • Serve as liaison between the sponsor and PPD 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 • Interact with investigators and answer IRB and Health Authority questions • 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 medical compliance by applying relevant SOPs and GCP • Collaborate with cross-functional study team members on medical risks, issues, and results

🎯 Requirements

• Medical Doctor with a specialty in Pulmonology • Clinical experience treating pulmonology patients in hospital practice • 1–2 years of industry experience in clinical development • Significant experience within the pharmaceutical industry, clinical trials, and pharmaceutical medicine • Fluent spoken and written English • Understanding and experience with NDA submission processes • Understanding of regulatory guidelines for adverse event reporting • Strong communication and presentation skills • Strong teamwork skills

🏖️ Benefits

• Meaningful work making a positive impact on a global scale • Resources to achieve individual career goals • Work with life-changing therapies and clinical research services • Equal employment opportunity and affirmative action • Diverse experiences, backgrounds, and perspectives valued • Standard Monday–Friday schedule

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