Regulatory Affairs Associate

CK Group are recruiting for a Regulatory Affairs Associate to join a leading global helathcare company on a contract basis until December 2026. This is a hybrid role with 2 days per week in Reading.

Salary:
From £25 ph PAYE

Regulatory Affairs Associate Role:

Support and maintain pharmaceutical product portfolios
Manage ongoing product information updates
Supports regulatory project plan execution
Assist in the preparation and review of labelling and local SOPs
Compile regulatory documents for submission

Your Background:

Hold a relevant scientific degree or have equivalent working experience
Good knowledge and experience of UK regulations
Previous working experience in pharmaceutical regulatory affairs
Ability and experience to work cross-functionally with different functions involved:
Global functions, QA, PV, Marketing
Excellent communication skills
Any project management experience would be an advantage

Company:
Our client is one of the worlds leading healthcare providers, and has been highly innovative in providing healthcare solutions, to unmet medical needs through scientific advancement as well as strategic acquisitions and partnerships. They work at the critical intersection where innovations that save and sustain lives meet the physicians, nurses and pharmacists who make it happen. Our client is committed to improving outcomes for patients, and helping their partners meet the evolving challenges and opportunities in healthcare around the world.
 
Apply:
For more information, or to apply for this Regulatory Affairs Associate please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).

It is essential that applicants hold entitlement to work in the UK

Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check