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Senior Pharmacovigilance Officer
Surrey
Permanent opportunity
Are you seeking a change from working with large corporations? Do you have extensive experience in pharmacovigilance? If so, we want to hear from you!
If making a meaningful impact every day within a dynamic small business excites you, then we have the perfect opportunity for you. We value innovation, agility, and a collaborative environment where your contributions are recognized and appreciated. Say goodbye to the "stuffiness" of large corporations and join our team where you can thrive and grow.
We seek an accomplished Senior Pharmacovigilance Officer with a proven track record in the discipline. Your proficiency in adverse drug reactions and risk management is paramount to us. Join our team and contribute your expertise to advance patient safety and public health initiatives. With multiyear operations in the UK, EU, and selected global markets, we offer a dynamic environment to excel in.
Key Responsibilities
- Responsible for reviewing Technical Agreements and managing PV contracts from start to finish.
- Daily oversight and monitoring of two PV and two MI mailboxes.
- Maintains the UK and EU PSMFs.
- Maintains the Risk Management Plans.
- Managing and updating the Deviation/CAPA tracker.
- Ensure that PV and MI Standard Operating Procedures (SOPs) are compliant, align with company requirements, and remain up to date.
- Managing and processing monthly MI reconciliation reports received from partners.
- In this global position, you will serve as the primary contact for pharmacovigilance (PV) matters and additionally offer management information (MI) support for the business. Submitting weekly MI reconciliation reports to the PV vendor.
Qualifications
- Preferably possessing a minimum of five years of experience within the pharmacovigilance (PV) sector and actively engaged in PV audits/inspections.
- To be able to self-manage
- Proficient with Microsoft
- Educated to a degree,( preferably in the Life Sciences field.)
- Demonstrated strong leadership skills, with proven ability in team building and inspiring teams.
- Possessing extensive knowledge of local/UK and EU pharmacovigilance (PV) regulatory requirements. Additionally, having a comprehensive understanding of drug safety methodologies to ensure compliance standards are met in signal detection and evaluation, risk/benefit assessments.
If you do not hear back from Projectus within 7 days of your application please assume it has been unsuccessful on this occasion only.
