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
What you'll do:
- 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 ArisGlobal
- Support the UK QPPV and PSMF maintenance where required
What you'll bring:
- 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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Pharmacovigilance Specialist | Contract | Reading employer: Myn
Myn is an exceptional employer, offering a nurturing and supportive work environment for Nursery Room Leaders in Bristol. With generous benefits such as 33 days of annual leave, flexible working options, and extensive family and wellbeing support, employees are encouraged to thrive both personally and professionally. The company prioritises employee growth through tailored training and progression opportunities, making it a rewarding place to build a meaningful career in early years education.
