Regulatory Affairs Specialist

1 month ago


Uxbridge, United Kingdom CK Group- Science, Clinical and Technical Full time
Senior Associate Regulatory Affairs

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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