Regulatory Operations Associate
12 month contract
Remote
£25-£27 per hour
Cpl Life Sciences are continuing the partner with a large global pharmaceutical company into 2023 and supporting the expansion of their Regulatory Operations team. They are seeking two individuals both who will be working directly on Veeva Vault and with working knowledge of Regulatory Information Management. Strong working knowledge of the drug development process and regulatory submission management is desirable for this role, as well as direct experience with Veeva Vault.
Key responsibilities shall include:
- Ensure Clinical Trial Submissions are compliance and submitted to the relevant EU bodies
- Coordinate the Clinical Trial Applications to ensure timely input and submission
- Oversee the compliance of relevant CTA’s
- Assist with the development and implementation of existing and evolving policies and processes
- Work on Veeva Vault and the Regulatory Information Management system
- Maintain all relevant tracking systems
- Raise and resolve any issues that may impact submission timelines
If you have an interest in Regulatory Operations and have experience with submissions on Veeva Vault then this position would be a great opportunity within the pharmaceutical industry.
If this role as a Regulatory Operations Associate is of interest then please apply here, or alternatively send your CV directly to [email protected].