Pharmacovigilance Manager
CV-LibraryWoking, SurreypermanentPosted: 30 July 2026
Apply NowPharmacovigilance & Scientific Information Manager
I'm partnering with a long-standing client that we've successfully supported across the business for a number of years. What continues to stand out is the culture: a genuinely collaborative environment, small teams, approachable leadership, and the opportunity to have real influence. This isn't a large corporate structure where you're one of many. Instead, you'll work directly with international affiliates in a visible function that offers high potential.
As Pharmacovigilance & Scientific Information Manager, you'll take ownership of PV activities across the UK & Ireland, acting as the local PV lead and UK Contact Person (NCPP) while leading a small team. The role offers an excellent blend of strategic responsibility and hands-on involvement, giving you the opportunity to work across pharmacovigilance, scientific information, inspections, compliance, and stakeholder management on a daily basis.
What you'll be doing
* Leading Pharmacovigilance activities across the UK & Ireland.
* Acting as the UK Contact Person for Pharmacovigilance (NCPP).
* Managing and developing a small Scientific Affairs team.
* Working closely with global PV and Medical Affairs colleagues.
* Maintaining oversight of Medical Information activities.
* Supporting inspections, audits, compliance, and continuous improvement initiatives.
What we're looking for
* Strong Pharmacovigilance experience within the pharmaceutical industry.
* Solid understanding of UK PV regulations, MHRA requirements, and GVP.
* Previous people management or team leadership experience is essential – even if of small teams focusing on coaching and development
* Experience in scientific/medical information desirable
* Portfolio experience is less important – but experience (or a desire and capability) to deal with a large portfolio is key
* Confidence working across multiple stakeholders and international teams.
* A proactive, hands-on approach and the ability to thrive in a collaborative environment.
For further details, please contact Mark Bux-Ryan.
PV, pharmacovigilance, medical, scientific, information, safety, drug, adverse, event, MHRA, regulatory, leader, manager, supervisor, head, affairs
I'm partnering with a long-standing client that we've successfully supported across the business for a number of years. What continues to stand out is the culture: a genuinely collaborative environment, small teams, approachable leadership, and the opportunity to have real influence. This isn't a large corporate structure where you're one of many. Instead, you'll work directly with international affiliates in a visible function that offers high potential.
As Pharmacovigilance & Scientific Information Manager, you'll take ownership of PV activities across the UK & Ireland, acting as the local PV lead and UK Contact Person (NCPP) while leading a small team. The role offers an excellent blend of strategic responsibility and hands-on involvement, giving you the opportunity to work across pharmacovigilance, scientific information, inspections, compliance, and stakeholder management on a daily basis.
What you'll be doing
* Leading Pharmacovigilance activities across the UK & Ireland.
* Acting as the UK Contact Person for Pharmacovigilance (NCPP).
* Managing and developing a small Scientific Affairs team.
* Working closely with global PV and Medical Affairs colleagues.
* Maintaining oversight of Medical Information activities.
* Supporting inspections, audits, compliance, and continuous improvement initiatives.
What we're looking for
* Strong Pharmacovigilance experience within the pharmaceutical industry.
* Solid understanding of UK PV regulations, MHRA requirements, and GVP.
* Previous people management or team leadership experience is essential – even if of small teams focusing on coaching and development
* Experience in scientific/medical information desirable
* Portfolio experience is less important – but experience (or a desire and capability) to deal with a large portfolio is key
* Confidence working across multiple stakeholders and international teams.
* A proactive, hands-on approach and the ability to thrive in a collaborative environment.
For further details, please contact Mark Bux-Ryan.
PV, pharmacovigilance, medical, scientific, information, safety, drug, adverse, event, MHRA, regulatory, leader, manager, supervisor, head, affairs