CK Group are recruiting for a Clinical Trial Associate to join a global pharmaceutical company, based in Slough, on a contract basis initially for 12 months.
Salary: Hourly: 20.03 PAYE or 27.27 via Umbrella.
Clinical Trial Associate Role:- Develop a Trial Master File (TMF) Plan, conduct ongoing and final Quality Control (QC) checks of TMF.
- Support audit/inspection activities and support Clinical Development Quality Lead (CDQL).
- Act as subject matter expert on client systems and continue to find efficiencies between client systems and Partner systems.
- Participate in Clinical Study Team meetings and/or other trial-related meetings when specific expertise is required.
Your Background:
- Hold a relevant scientific degree or have equivalent working experience.
- Previous experience with creating Trial Master Files within the pharmaceutical industry.
- Excellent communication skills.
- Excellent eye for detail.
Company: Our client is a is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location: This role is based at our clients site in Slough.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 106428 in all correspondence.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.