CK Group are recruiting for a Senior Associate Regulatory Affairs to join a biopharmaceutical company remotely on a contract basis for 12 months.
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.
This Senior Associate Regulatory Affairs role will home based and post covid candidate will be required to work from the Uxbridge site.
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.
- Strong written and communication skills
- Degree in life sciences, biochemistry, or chemistry
- Proactive nature
- Experience in biopharmaceutical or pharmaceutical industry preferable
- CMC experience preferable
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
Website: CK Group
- Posted: 14th January 2021
- Expires: 11th February 2021