Senior Associate Regulatory Affairs
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 Uxbridgesite.
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 responsiblefor 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.
- 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: For more information or to apply for this Senior Associate Regulatory Affairs position, please contact Lucy on 01438 870011 or email email@example.com, quoting job ref 49607.
It is essential that applicants hold entitlement to work in the UK.