Pharmacovigilance Specialist - Contract - Reading

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 ICSRs 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. Interested? Apply via the link or message the Myn team for a confidential conversation.