Pharmacovigilance Specialist
Cpl · Reading, Berkshire
Pharmacovigilance Specialist at Cpl, based in Reading, Berkshire, paying £25.00 - £35.00 per hour. This is a contract role with hybrid working.
- Salary
- £25.00 - £35.00 per hour
- Location
- Reading, Berkshire · Hybrid
- Contract
- Contract
- Posted
- 23 hours ago
- Closes
- 17 Nov 2026
- Sector
- Science & Pharmaceutical
48% below the typical rate for science & pharmaceutical
Reference uk/jobs/976434598
About the role
Pharmacovigilance Specialist – UK & Ireland
Cpl Life Sciences are working with an established pharmaceutical business that is seeking a Pharmacovigilance Specialist to join its team, supporting the delivery of high-quality pharmacovigilance activities across the UK and Ireland.
This is an excellent opportunity for an experienced PV professional to join a pharmaceutical environment where you will play an important role in ensuring the effective management of safety information and compliance with applicable pharmacovigilance requirements.
Overview:
- £25-35 per hour PAYE
- Hybrid working in Berkshire (2-3 days per week on site)
- Initial 9 month contract
Key Responsibilities:
- Manage Pharmacovigilance activities, including the end-to-end handling and processing of safety reports at affiliate level.
- Process individual case safety reports accurately and within required timelines using a safety database.
- Support compliance with UK and Ireland Pharmacovigilance requirements and relevant post-Brexit regulatory changes.
- Contribute to post-authorisation Pharmacovigilance activities for medicinal products.
- Ensure safety cases and associated documentation are maintained to a high standard.
- Work closely with the PV Manager and wider internal stakeholders to support ongoing safety activities.
- Manage competing priorities effectively while maintaining accuracy and meeting regulatory deadlines.
Experience & Skills Required:
- Experience managing safety reports through an end-to-end process at affiliate level.
- Experience within a pharmaceutical or life sciences environment.
- A degree in a relevant scientific discipline is preferred.
- Good knowledge of post-authorisation requirements for medicinal products.
- Understanding of post-Brexit Pharmacovigilance regulations impacting the UK and Ireland.
- Experience with ARGUS at UK affiliate level would be advantageous but is not essential.
- Strong attention to detail and the ability to work effectively under pressure and to tight deadlines.
- Good working knowledge of Microsoft Office.
Reporting to: PV Manager
This is a great opportunity for a Pharmacovigilance professional looking to develop their career within a pharmaceutical organisation and take on a role with responsibility across the UK and Ireland.
Reference: uk/jobs/976434598 · Posted 23 hours ago · Closes 17 Nov 2026 · Listed via Cpl
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