Clinical Trials Coordinator
4 weeks ago
CK Group is seeking a Clinical Trial Associate to support a leading global pharmaceutical organization on a contract basis.
Compensation:
Hourly rate: £20.03 PAYE or £27.27 via Umbrella.
Key Responsibilities:
- Establish and maintain a comprehensive Trial Master File (TMF) Plan, ensuring ongoing and final Quality Control (QC) assessments of the TMF.
- Assist in audit and inspection preparations while collaborating with the Clinical Development Quality Lead (CDQL).
- Serve as a subject matter expert on client systems, continuously seeking efficiencies between client and partner systems.
- Engage in Clinical Study Team meetings and other trial-related discussions when specialized knowledge is required.
- Possess a relevant scientific degree or equivalent professional experience.
- Demonstrated experience in creating Trial Master Files within the pharmaceutical sector.
- Exceptional communication skills.
- Strong attention to detail.
Our client is a prominent biopharmaceutical company dedicated to enhancing the lives of individuals affected by severe diseases in the fields of immunology and neurology.
Important Note:
Applicants must have the right to work in the UK. This position may require a satisfactory basic Disclosure and Barring Service (DBS) check.
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