Regulatory Affairs Specialist
1 month ago
CK Group- Science, Clinical and Technical is seeking a highly skilled Senior Associate Regulatory Affairs professional to join their team on a 12-month contract basis.
About the Role:
This is an exciting opportunity to provide European regional regulatory leadership and expertise for the development, registration, and lifecycle management of medicinal products.
Key Responsibilities:
- Execute the regional regulatory strategy and regional regulatory plans.
- Prepare supportive documentation for regulatory deliverables, including the management of clinical trial applications, marketing authorisations, and lifecycle management activities.
- Build effective relationships and communication paths across local and functional organizations.
Requirements:
To be successful in this role, you will need a Master's degree in a scientific area or a Bachelor's degree in a scientific area with 2 years of directly related experience. You should also have in-depth knowledge of regional countries legislation and regulations relating to medicinal products, as well as experience with Market Authorisations.
What We Offer:
CK Group- Science, Clinical and Technical offers a competitive hourly rate of up to £32.29 Umbrella / £24.57 PAYE, as well as the opportunity to work with a global pharmaceutical company and contribute to the development of innovative human therapeutics.
Location:
The role is hybrid, with the office team locations in Uxbridge and Cambridge. We are looking for candidates in this vicinity who can work effectively in a remote setting.
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