At a Glance
- Tasks: Manage submissions for clinical trials and marketed products while ensuring compliance with regulations.
- Company: Join Amgen, a leading biotechnology company in the UK.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on innovation and compliance.
- Why this job: Play a key role in shaping regulatory strategies and optimising development programmes.
- Qualifications: Experience in regulatory affairs and strong collaboration skills required.
The predicted salary is between 60000 - 80000 £ per year.
Amgen in the United Kingdom seeks a Regulatory Affairs professional to manage submissions for clinical trials and marketed products.
You will support regional regulatory activities, implement national plans, and guide documentation and meetings in line with global strategies.
You will ensure compliance with changing regulations, collaborate across functions, and help optimize development programs, including expedited and special pathways.
We think you need these skills to ace Regional Regulatory Affairs Manager-Submissions & Strategy in Uxbridge
Regulatory Affairs
Clinical Trials Management
Submission Management
Compliance Knowledge
Documentation Skills
Strategic Planning
Cross-Functional Collaboration
