Senior Safety Specialist
Thermo Fisher Scientific · Remote, Serbia · Global
Regulatory Affairs
Remote
Not yet analysed
Demand70
Career growth62
Healthcare fit72
Remote potential55
5-year outlook
Pharmacovigilance pay typically starts modest for case-processing roles and rises with experience in signal management, aggregate reporting, or safety lead positions. Senior-level safety roles generally offer stable, mid-to-upper pharma-services compensation, though exact figures vary by location and are not stated here.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
–
Date found
2026-10-21
Intelligence details
Why this is worth applying to
Worth considering if you already have pharmacovigilance or clinical safety exposure and want a stable pharma-services career; clinicians without PV experience will likely find the 'Senior' bar hard to clear without a stepping-stone role.
Who should apply
Pharmacists with PV case-processing or medical information experience, nurses or doctors who have worked in drug safety, clinical trial safety, or medical affairs, and IMGs with prior CRO/pharma safety exposure.
CV angle
Reframe real clinical experience into safety language: adverse drug reaction recognition and reporting, medication reconciliation, patient narrative summarisation, triage and prioritisation under time pressure, and familiarity with MedDRA-style coding concepts. Highlight any SOP-driven documentation, regulatory or audit exposure, and quality/CAPA work — do not claim PV systems experience you do not have.
Skills to highlight
- Adverse event / ADR identification and reporting
- Clinical narrative summarisation and case documentation
- Medication and pharmacology knowledge
- Regulatory and SOP compliance
- Attention to detail and data accuracy
- Triage and prioritisation under caseload pressure
- Cross-functional communication with medical and quality teams
Role summary
A senior pharmacovigilance/drug safety position at a large pharma services organisation, likely involving review and processing of adverse event reports, safety documentation, regulatory-compliant reporting timelines, and possibly signal support or mentoring of junior safety staff.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.