Clinical Trials Associate

Exciting Opportunity: Clinical Trials AssociateAre you a detail-driven clinical professional with hands-on experience supporting clinical trials? We are seeking a Clinical Trials Associate to join a growing team and play a key role in managing Trial Master File (TMF) activities and supporting the delivery of clinical studies. Job Title: Clinical Trials Associate Vacancy Type: Permanent Location: Hertfordshire Salary: DOEWorking type: 5 days on site until passing probation - then 3 days on site.Special considerations: due to location and unreliable public transport, you would need to either have a driving license and car or be comfortable taking alternative modes of transportation (cycling). Sponsorship is unavailable for this role. The Role of the Clinical Trials AssociateAs a Clinical Trials Associate, you will support the successful delivery of clinical studies through effective coordination, documentation management, and administrative support. A core focus of this role will be ownership and maintenance of the TMF, ensuring compliance with regulatory standards and inspection readiness.Key responsibilities include:Managing Trial Master File (TMF) activities, including set-up, maintenance, QC checks, and archivingEnsuring TMF completeness, accuracy, and inspection readiness throughout the study lifecycleSupporting clinical trial administration across study start-up, conduct, and close-out activitiesPreparing and maintaining study documentation, meeting minutes, and tracking ..... full job details .....