Clinical Trial Manager
400-500 per day (PAYE)
London office: 1-2 days on site required
Cpl are currently recruiting for an experienced Clinical Trial Manager on behalf of a global pharmaceutical company to have oversight of several clinical trials ranging from phase I-IV. The studies will be across a range of therapy areas and on both a global and regional level.
The successful trial manager will have oversight of trial deliverables as well as CRO and vendor oversight and management. Experience of previous CRO oversight would be a strong advantage for this role.
The position is a full time role offering hybrid working with the expectation to be on site 1-2 days per week in London.
Key experience and responsibilities include:
Oversight of both regional and global studies.
Operational trial management from study start-up to close out.
Experience with managing and overseeing vendor relationships and performance.
Tracking and review of vendor performance.
Ensure the trials are conducted on time, within cost and to the highest quality.
Oversee the study level budget and relevant invoices.
Provide input into clinical documents including monitoring plans and reports.
Liaise cross-functionally to ensure data management and review is to standard.
Participate in SOP development and tracking.
Strong knowledge of GCP and FDA regulations and guidelines.
Experience within a pharmaceutical or biotech setting.
If you are an experienced trial manager looking for a new opportunity to work across a number of studies then please apply here or email email@example.com with your CV for further information.
- Agency: Cpl Life Sciences
- Contact: Sarah Phillips
- Reference: JO-2109-476151
Website: Cpl Life Sciences
- Posted: 13th September 2021
- Expires: 11th October 2021