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Clinical Research Associate
1 month ago
Slough, Slough, United Kingdom CK Group Full timeClinical Trial Associate RoleCK Group is seeking a skilled Clinical Trial Associate to join a global pharmaceutical company in Slough, UK, on a contract basis for 12 months.Key Responsibilities:Develop and maintain Trial Master Files (TMFs) and conduct quality control checks.Support audit and inspection activities, and collaborate with the Clinical...
Clinical Trial Associate
3 months ago
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.
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.