Pharmacovigilance Specialist
Job Description & How to Apply Below
We're recruiting a Pharmacovigilance Specialist for a contract role in a drug safety team. You'll handle adverse event reporting and support aggregate reporting and signal management, keeping the team compliant with MHRA, EU and ICH pharmacovigilance requirements.
Location:
Reading, UK
Day rate: £350–£450 per day (IR35 status to be confirmed)
Contract:
Initial 6–12 months, likely extension
- Process ICDSRs from receipt to submission, including MedDRA/WHODrug coding and narrative writing
- Manage expedited reporting to the MHRA and other regulators within legislative timelines
- Support PSURs/PBRERs, DSURs and RMPs
- Contribute to signal detection, literature screening and safety database review
- Maintain safety databases such as Argus and Aris Global
- Support the UK QPPV and PSMF maintenance where required
- Life sciences or healthcare degree (Pharmacy, Nursing, Biology, Pharmacology, Medicine)
- 3–6 years' pharmacovigilance experience in pharma, biotech or CRO environments
- Hands‑on ICSR processing experience and working knowledge of GVP Modules
- Proficiency with safety databases and MedDRA coding
- Right to work in the UK
Desirable: aggregate reporting or signal management experience, MHRA PV inspection support, medical device vigilance, CRO/vendor oversight.
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