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Senior Associate Regulatory Affairs

UK   •  Contract/Temporary, Full time


CK Group are recruiting for a Senior Associate Regulatory Affairs to join a biopharmaceutical company remotely on a contract basis for 12 months.

Company:
Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics.

Location:
This Senior Associate Regulatory Affairs role will home based and post covid candidate will be required to work from the Uxbridge site.

Salary:
Competitive.

Senior Associate Regulatory Affairs Role:
The Senior Associate Regulatory Affairs (CMC) provides varying levels of product support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across phases of product development from clinical to lifecycle. Support may include organizing, managing and executing on regulatory CMC projects and submissions. Tasks may include creating and/or maintaining submission timelines and tables of contents, formatting of documents per style guide, scheduling meetings, drafting meeting agendas and minutes, managing document reviews and other tasks as requested.

Background:

  • Strong written and communication skills
  • Degree in life sciences, biochemistry, or chemistry
  • Proactive nature
  • Experience in biopharmaceutical or pharmaceutical industry preferable
  • CMC experience preferable

Apply:
Quote job ref 49607.

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


You must be eligible to work in the UK. Learn more

  • Agency: CK Group
  • Contact: Lucy Stendall
  • Phone: 01246 457733
  • Reference: 49607
  • Posted: 14th January 2021
  • Expires: 11th February 2021

CK Group

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