Filter Results

  • Filter by Pay
  • Filter by Job Type
  • Filter by Working Pattern
  • Filter by Distance From
  • Filter by Industry

Discover new job roles in East England, United Kingdom

View Saved Jobs (0)
View Saved Jobs (0)

Regulatory Affairs Manager UK and Ireland

4792787
Apply Now
Save Job

  • Job type

    Contract

  • Location

    Cambridge / Remote

  • Working Pattern

    Full-time

  • Specialism

    Life Sciences Manufacturing

  • Industry

    Scientific and R&D

  • Pay

    Inside IR35

  • Closing date

    30 Jun 2026
Share Job

Regulatory Affairs Manager Conract– UK & Ireland Affiliate

Your new company

You’ll be joining a leading, research‑driven biopharmaceutical organisation with a strong UK & Ireland presence and large global footprint. The business manages a robust portfolio of centrally approved medicines and continues to invest in regulatory capability to support post‑approval lifecycle management and commercial growth across the UK&I markets.

Your new role

This is a Regulatory Affairs Manager mat cover position on a 12‑month contract, with the possibility of extension. The role sits within the UK & Ireland Regulatory Affairs function, reporting into the Head of UK Regulatory Affairs within the affiliate team.

The position will focus on post‑approval regulatory activities for centrally authorised (CP) products, with close collaboration across UK & Ireland stakeholders. The role will primarily support products within RRMS and will involve managing complex regulatory deliverables.

Key responsibilities may include:
  • Post‑approval lifecycle management (LCM) activities for UK & Ireland
  • Management of complex Type II and other significant variations
  • Regulatory support for Paediatric Investigation Plans (PIPs)
  • Involvement in clinical trial regulatory activities
  • Review and approval of promotional and non‑promotional materials
  • Use of Veeva regulatory information management systems

What you'll need to succeed

  • Demonstrated experience with complex variations, including Type II
  • Proven experience in UK & Ireland affiliate regulatory affairs
  • Strong post‑MAA lifecycle management expertise for CP products
  • Exposure to PIPs and clinical trial regulatory submissions
  • Experience working with Veeva or similar regulatory systems
  • Excellent communication skills and confidence working cross-functional
  • A collaborative, hands-on approach with a willingness to support across the wider team


The ideal start date is end of July / early August, and candidates should be local to, or able to attend, the Cambridge office once per month.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden for a confidential discussion about your career.