Regulatory Affairs Manager - Leading Global Biopharma | UKYour new company
Our client, a leading global biopharmaceutical organisation, is dedicated to advancing science and improving patient lives. With people at the heart of every decision, they are committed to ensuring patients today and for generations to come receive the treatments they need.We are supporting them in the search for an exceptional Regulatory Affairs Specialist to join their UK organisation and play a pivotal role in shaping strategic regulatory initiatives.
Your new role
As a Regulatory Partner, you will be a key member of the UK Regulatory function, providing expert guidance and strategic direction across a broad portfolio. You'll collaborate cross-functionally to influence policy, accelerate access to innovative medicines, and ensure the company maintains a strong licence to operate in the UK.This is a unique chance to make a tangible impact on patient outcomes within a mission driven, science led environment.
Working within the UK Regulatory Group, you will:
1. Navigate and translate evolving UK regulatory requirements into business ready solutions.
2. Lead or support:
3. Clinical Trial Applications
4. National Licencing Applications
5. Early Access to Medicines submissions
6. National components of centralised EU procedures
7. Act as a primary point of contact with the MHRA...