Regulatory Affairs Principal Specialist

1 day ago


Crawley, United Kingdom CK GROUP Full time

CK Clinical are recruiting for a Regulatory Affairs Principle Specialist to join a specialist Clinical Research Organisation on either a permanent or contract basis. The duration of the contract would initially be set to 6 months.
**Location**:
The client is based in Crawley and would ideally like someone who is open to working on a hybrid model, with a couple of days in the office a week. However, there is some flexibility on this, so if you are looking for remote work don't hesitate to get in touch.
**Salary**:
**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 53693 in all correspondence.



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