At a Glance
- Tasks: Lead regulatory activities for clinical trials in Immunology, Inflammation, and Genetics.
- Company: Join a leading global biotechnology organisation making a difference.
- Benefits: Competitive salary, flexible working, and opportunities for professional growth.
- Other info: 12-month contract based in vibrant West London.
- Why this job: Be at the forefront of clinical development and impact patient lives.
- Qualifications: Strong European clinical regulatory expertise and experience in managing applications.
The predicted salary is between 60000 - 80000 £ per year.
Cpl Life Sciences is partnering with a leading global biotechnology organisation to recruit an experienced Senior Manager, Regulatory Affairs to support a growing portfolio of clinical development programmes across Immunology, Inflammation and Genetics. This 12-month contract role is based in West London and is ideal for a regulatory professional with strong European clinical regulatory expertise.
The successful candidate will own clinical trial applications and lead regulatory activities.
European Regulatory Affairs Lead — Clinical Trials (12‑Month Contract) employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the vibrant streaming and entertainment sector. Employees benefit from immediate project impact opportunities, comprehensive training, and career growth in a cloud-oriented environment, making it an ideal place for those looking to advance their skills in data engineering while working with cutting-edge technologies.
