Regulatory Affairs Specialist
2 months ago
CK Group is seeking a highly skilled Regulatory Affairs Manager to join a global pharmaceutical company on a 12-month contract basis, based in Uxbridge. This is a unique opportunity to work with a company committed to unlocking the potential of biology for patients suffering from serious illnesses.
About the CompanyOur client is a leading pharmaceutical company dedicated to discovering, developing, manufacturing, and delivering innovative human therapeutics. They utilize advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.
Key Responsibilities- Develop and execute regional regulatory strategies and plans.
- Prepare and manage regulatory deliverables, including clinical trial applications, marketing authorizations, and lifecycle management activities.
- Build and maintain effective relationships and communication paths across local and functional organizations.
- Master's degree in a scientific area or Bachelor's degree in a scientific area with previous directly related experience.
- Depth knowledge of regional countries' legislation and regulations relating to medicinal products.
- Experience with Market Authorizations, CTAs, post-approval changes, and amendments, extensions, and renewals.
Competitive hourly rate of up to £43.94 PAYE. The role is hybrid, with office locations in Uxbridge and Cambridge. We are looking for candidates in this vicinity.
Please note that it is essential to hold entitlement to work in the UK. Please quote reference 107533 in all correspondence.
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