Trial Co-ordinator

Prepare and submit in a timely manner all required study reports (progress, safety (for CTIMPS), end of study). Collect and report safety information according to MYTT established procedures Liaise between researchers and CLRN to ensure efficient returns regarding recruitment/study progress and any additional funding required. Sourcing, ordering from appropriate research budgets, and distribution of clinical supplies (e.g. blood tube, reagents etc), stationery or equipment Coordinate the receipt, transfer and storage of any clinical materials or biosamples collected during the study in accordance with GCP guidelines.

Identify training and resource needs for research staff and provide appropriate support to ensure efficient trial progress. Coordinate adverse event reporting processes and monitor timelines for accuracy of SAE reports. Monitor the timelines, accuracy, and quality of CRFs and data return Prepare and liaise with appropriate staff for monitoring visits, audits or statutory GCP, inspection by the MHRA or any other body. Ensure timely implementation and completion of any corrective and preventive actions required, working with quality manager as needed Ensuring agreed recruitment metrics are achieved within the agreed timeline Identify barriers to participation in trials and develop strategies with clinicians, Trusts and others to overcome these barriers.

Publicising current trials to encourage new participants to join, and to maintain enthusiasm amongst existing participants by appropriate methods - mainly personal letters and the production of regular newsletters for specific projects.