Senior Medical Director, Medical Monitor

🔥 2 hours ago

🇹🇼 Taiwan – Remote

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

👻 Ghost score 12%

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

• Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed • Attends and presents at investigator and sponsor meetings • Provides medical consultation to clients, investigators, and project team members • Supports business development activities • Manages medical aspects of contracted tasks across the pharmaceutical product life-cycle • Ensures tasks delegated to Pharmacovigilance are properly executed • Provides medical consultation and answers study-related medical questions • Provides therapeutic and protocol training on assigned studies • Writes and/or reviews CSRs, IND/NDA reports, ICSRs, signal detection reports, periodic reports, RMPs, REMS, and CTD modules • Contributes to departmental process improvement initiatives • Monitors safety variables including adverse events, laboratory abnormalities, patient medical status, concomitant medications, and un-blinding requests • Discusses medical concerns with principal investigators and clients and applies medical judgment to clinical situations • Reviews adverse events of special interest, serious adverse events, and clinical outcome events • Performs data review and validation, including coding listings and/or full safety data, to assess potential safety concerns • Manages signal detection activities and generates aggregate reports • Contributes to label updates, dossier maintenance, and risk management activities • Medically reviews adverse-event and serious-adverse-event data from solicited, spontaneous, literature, and other sources • Serves as a consultant and spokesperson for the functional area or organization on significant matters • Creates formal networks with key decision makers

🎯 Requirements

• MD or equivalent required • Active medical licensure preferred • Clinical experience treating patients in hematology oncology or a related subspecialty, comparable to 2 years • Suitable clinical trial experience in a contract research organization, pharmaceutical company, or as a principal investigator, comparable to 1–2 years; or direct experience in safety/Pharmacovigilance, comparable to 2 years • Knowledge of applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues • Ability to adhere to client SOPs/directives, project-specific WPDs, and corporate policies and SOPs/WPDs • Ability to exercise independent judgment in methods, techniques, and evaluation criteria • Broad expertise or unique knowledge to contribute to company objectives and principles • Ability to develop solutions to highly complex and unique issues

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule

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