At a Glance
- Tasks: Support patient safety and regulatory compliance in pharmacovigilance activities.
- Company: Join a respected, innovation-driven consumer healthcare organisation.
- Benefits: Hybrid work model, competitive salary, and opportunities for career growth.
- Other info: Collaborative team environment with a focus on continuous improvement.
- Why this job: Make a real impact on patient safety and contribute to global healthcare.
- Qualifications: Experience in pharmacovigilance and strong attention to detail.
The predicted salary is between 35000 - 45000 £ per year.
Carrot Recruitment is delighted to be partnering with a highly respected, innovation-driven consumer healthcare organisation to appoint a Pharmacovigilance Officer. This role will be offered as either a contracted fixed term until June 2027 or as a temporary contract with an initial 6 month term with possibility to extend or switch to permanent, depending on business need.
The Pharmacovigilance Officer position is a full time hybrid opportunity based in Coventry (3 days in office Tuesday-Thursday), offering the chance to join a collaborative and forward-thinking team supporting UK, European and global pharmacovigilance and vigilance activities across a diverse product portfolio. If you’re passionate about patient safety, regulatory excellence and continuous improvement, this could be a fantastic next step in your PV career.
Everything You Need to Know About This Role
As a Pharmacovigilance Officer, you will support a broad range of PV activities, ensuring compliance with regulatory requirements and maintaining high standards of patient safety. Key responsibilities include:
- Monitoring and triaging Individual Case Safety Reports (ICSRs)
- End-to-end ICSR processing (including MedDRA coding, seriousness assessment, database entry and expedited reporting)
- Supporting signal management, risk management plans and periodic safety reports (PSURs/PBRERs)
- Maintaining SDEAs and supporting reconciliation activities
- Contributing to PSMF updates, audits, CAPAs and self-inspections
- Supporting PV compliance for new product launches and licence changes
- Delivering PV training and monitoring regulatory updates
You will work closely with cross-functional teams including Medical Information and Operations, contributing to continuous improvement initiatives.
