Clinical Trial Associate

Clinical Trial AssociateCK 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 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.