At a Glance
- Tasks: Lead European regulatory activities for clinical programmes and manage interactions with CROs.
- Company: CPL Life Sciences, a leader in regulatory affairs within the life sciences sector.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Other info: 12-month contract with potential for career advancement in a dynamic environment.
- Why this job: Make a significant impact on clinical trials in Immunology, Inflammation, and Genetics.
- Qualifications: Experience in regulatory affairs and strong leadership skills required.
The predicted salary is between 100000 - 104000 £ per year.
CPL Life Sciences in the UK is seeking a Senior Manager, Regulatory Affairs to lead European regulatory activities for multiple clinical programmes.
The role focuses on CTAs, submissions, and strategic regulatory leadership across Immunology, Inflammation and Genetics portfolios.
The successful candidate will manage interactions with CROs and global teams, ensuring regulatory excellence throughout the trial lifecycle and accelerating development under a 12-month contract.
#J-18808-Ljbffr
European CTA Regulatory Lead — 12-Month Hybrid Contract employer: Cpl Healthcare
Flexsource NI is an exceptional employer, offering a supportive work culture that prioritises employee development and teamwork. As a Catering Supervisor in the Craigavon Area, you will benefit from comprehensive training opportunities, a focus on high standards of food quality, and the chance to make a meaningful impact on patient dining experiences. Join us for a rewarding career where your contributions are valued and recognised.
