CK Clinical are recruiting for a Regulatory Affairs Principle Specialist to join a specialist Clinical Research Organisation on a permanent basis.
Location:
The client is based in Crawley but the position can be fully remote.
Salary:
£45,000-£60,000 per annum
The Role:
- To provide regulatory input to all assigned projects.
- Management, preparation, assembly of the Master Core Dossier and submissions of European; Clinical Trial Authorisation Applications (CTAA), Country-level Informed Consent and other relevant documentation.
- Serves as key regulatory liaison for multi-continental project on behalf of the company.
Your Background:
- Bachelor?s degree required preferably in a life science field or equivalent.
- At least 4 years of industry experience in a regulatory role (preferred).
- Prior experience in a CRO/pharmaceutical environment preferred.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 55530 in all correspondence.
You must have the right to work in the UK. Learn more
- Agency: CK Group
- Reference: 55530
Website: CK Group
- Posted: 15th May 2023
- Expires: 12th June 2023
