Pharmacovigilance Manager at RBW Consulting
London, Queensland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

23 Nov, 26

Salary

0.0

Posted On

25 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Healthcare & Life Sciences

Description

About the job


Pharmacovigilance & 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 doingLeading 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 forStrong 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

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Responsibilities
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