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
Website: CK Group
- Posted: 14th January 2021
- Expires: 11th February 2021
