Drug Safety Specialist

🔥 11 minutes ago

🇵🇭 Philippines – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 15%

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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 day-to-day pharmacovigilance activities in a highly regulated environment • Participate in on-call duties for specific projects to ensure 24-hour case-intake coverage • Collect, monitor, assess, evaluate, research, and track safety information • Perform data entry, coding, adverse-event assessment, case review, follow-up, report tracking, and regulatory reporting • Review regulatory/pharmacovigilance publications and information sources • Maintain medical understanding of applicable therapeutic areas and disease states • Review cases for quality, consistency, and accuracy, including peer reports • Prepare and maintain regulatory safety reports • Assist with project implementation and coordination, including clinical trials and safety-monitoring committees • Present at client and investigator meetings • Review metrics and budget considerations • Mentor less experienced staff • Assist with departmental and project-specific procedures and processes • Prepare for and attend audits, kick-off meetings, and investigator meetings • Collaborate with project teams, clients, investigators, adverse-event reporters, and third-party vendors

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 2+ years of previous experience providing relevant knowledge, skills, and abilities • Equivalent combination of appropriate education, training and/or directly related experience may be considered • General understanding of pathophysiology and disease processes • Detailed knowledge of relevant therapeutic areas for adverse-event processing • Strong critical thinking and problem-solving skills • Good 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 • Exposure to Microsoft Office, including Outlook, Word, and Excel • Understanding of procedural documents and regulations • Ability to manage and prioritize 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 • Ability to perform 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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