Clinical Trial Specialist

2 weeks ago


Slough, Slough, United Kingdom CK Group Full time
Clinical Trial Associate Role

Clinical Trial Associate

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)

Key Responsibilities:

  • 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.

About the Company:

Our client 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 client's site in Slough.



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