Senior Safety Specialist
200510503Z Thermo Fisher Scientific Pte. Ltd. · Serbia
Clinical Research
Remote
Not yet analysed
Demand78
Career growth72
Healthcare fit72
Remote potential35
5-year outlook
Demand for experienced pharmacovigilance and safety professionals should remain steady, especially in CRO and pharma-services settings. Compensation typically grows with case-processing, signal/risk management, and regulatory leadership experience, though exact figures vary by location and employer.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-26
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying if you already have pharmacovigilance, drug safety, or clinical trial safety experience and want a regulated non-patient-care career path. Clinicians without prior PV experience may find the 5+ year comparable-experience barrier too high.
Who should apply
Pharmacists, nurses, or physicians with drug safety, adverse event reporting, clinical trial, or pharmacovigilance experience; clinical research professionals seeking a senior safety/PV role.
CV angle
Reframe real clinical experience around adverse event recognition, medical terminology and pathophysiology, safety documentation, regulatory timeline management, case quality review, cross-functional collaboration, and audit readiness. Quantify trial, site, case, or safety-report volumes only where genuinely applicable.
Skills to highlight
- Pharmacovigilance
- Adverse event reporting
- Case assessment and quality review
- Clinical trial safety
- Regulatory compliance
- Medical terminology and pathophysiology
- Cross-functional collaboration
- Microsoft Office and safety databases
Role summary
A senior pharmacovigilance role responsible for day-to-day drug-safety activities, including collecting, assessing, tracking, and quality-reviewing adverse event information, supporting clinical trial safety committees, mentoring staff, and ensuring regulatory compliance within strict timelines.
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