Senior Drug Safety Specialist – Night Shift

Job not on LinkedIn

🔥 10 minutes ago

🇵🇭 Philippines – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 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

• Perform and potentially oversee day-to-day Pharmacovigilance activities in a highly regulated environment • Collect, monitor, assess, evaluate, research, and track safety information • Collaborate with project team members, clients, investigators, adverse-event reporters, and third-party vendors • Participate in on-call duties for specific projects to ensure 24-hour case-intake coverage • Lead activities and assist with developing program and departmental procedural documents • Prepare for and attend audits • Mentor less experienced staff • Review regulatory and pharmacovigilance publications and information sources • Maintain medical understanding of applicable therapeutic areas and disease states • Review cases, including peer reports, for quality, consistency, and accuracy • Coordinate routine project implementation, including clinical trials and post-approval activities • Present at client meetings and review metrics and budget considerations

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 5+ years of previous relevant experience • Thorough understanding of pathophysiology and disease processes • Strong knowledge of relevant therapeutic areas for adverse-event processing • Critical thinking and problem-solving skills, including appropriate evaluation and escalation • Proficiency in complex clinical study administration, budget activities, and forecasting • Excellent oral and written communication skills, including paraphrasing • Good command of English and ability to translate information into local language where required • Computer literacy and ability to work within multiple databases • Proficiency in Microsoft Office, including Outlook, Word, and Excel • Understanding of global regulatory requirements and compliance with procedural documents and regulations • Ability to manage and prioritize varied tasks and meet strict deadlines with limited supervision • Strong attention to detail • Ability to maintain a positive and professional demeanor in challenging circumstances • Ability to work effectively within a team • Willingness to work night/third-shift hours • Occasional domestic and international travel

🏖️ Benefits

• Collaboration and development opportunities • Opportunity to contribute to patient safety and scientific excellence • Global team environment • Occasional domestic and international travel

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