Negotiable
Undetermined
Undetermined
Cambridge, Cambridgeshire
Summary: You will be working as a Regulatory Affairs Manager for a prominent biopharmaceutical organization with a significant presence in the UK and Ireland. The role involves managing a portfolio of approved medicines and enhancing regulatory capabilities to support commercial growth. This position is contract-based and focuses on post-approval lifecycle management.
Key Responsibilities:
- Manage regulatory submissions and approvals for a portfolio of medicines.
- Support post-approval lifecycle management activities.
- Enhance regulatory capabilities to facilitate commercial growth.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
Key Skills:
- Experience in regulatory affairs within the biopharmaceutical industry.
- Strong understanding of UK and Ireland regulatory frameworks.
- Excellent communication and collaboration skills.
- Ability to manage multiple projects and deadlines effectively.
Salary (Rate): undetermined
City: Cambridge
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
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 click apply for full job details