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.

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 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.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.