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Trial Operations Specialist

2 months ago

Slough, United Kingdom CK Group- Science, Clinical and Technical Full time

CK Group is seeking a Clinical Trial Associate to support a leading global pharmaceutical organization on a contractual basis.


Compensation:

Hourly Rate:
£20.03 PAYE or £27.27 via Umbrella.

Key Responsibilities:
1. Develop and maintain a comprehensive Trial Master File (TMF) Plan.
2. Perform ongoing and final Quality Control (QC) assessments of the TMF.
3. Assist in audit and inspection activities, collaborating with the Clinical Development Quality Lead (CDQL).
4. Serve as a subject matter expert on client systems, identifying and implementing efficiencies between client and Partner systems.
5. Engage in Clinical Study Team meetings and other trial-related discussions where specialized knowledge is required.

Candidate Profile:
To be considered for this role, you should possess:
- A relevant scientific degree or equivalent professional experience.
- Prior experience in creating Trial Master Files within the pharmaceutical sector.
- Strong communication abilities.
- A keen attention to detail.

Company Overview:

Our client is a prominent global biopharmaceutical firm dedicated to delivering value for individuals affected by severe diseases in the fields of immunology and neurology.


Location:
This position is based at the client's site.

Application Process:
Applicants must have the right to work in the UK. Please reference the job code in all communications.

Note:
This position may require a satisfactory basic Disclosure and Barring Service (DBS) check.