At a Glance
- Tasks: Lead European regulatory activities for clinical trial applications and ensure compliance.
- Company: Cpl Life Sciences, a dynamic company in the heart of London.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: 12-month contract with potential for career advancement.
- Why this job: Make a significant impact on clinical trials and collaborate with global teams.
- Qualifications: Experience in regulatory affairs and strong communication skills.
The predicted salary is between 63000 - 77000 £ per year.
Cpl Life Sciences in London, UK is seeking a Senior Manager, Regulatory Affairs/Consultant (CTAs) for a 12‑month contract. Location: West London, Hybrid, with ASAP start.
You will own European regulatory activities for CTAs, submissions, health authority responses and regulatory maintenance, partnering with global development teams and external CROs to ensure compliance across programmes.
EU Regulatory Lead for Clinical Trials (CTAs) – Hybrid UK in England 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.
