Radiology Clinical Trials Coordinator

Job information Radiology Clinical Trials Coordinator from the Company The Christie NHS FT, this latest Radiology Clinical Trials Coordinator job vacancy is located in the city Manchester M. This latest job opening is open to job seekers who have the latest education / graduate . Job Vacancies in this Healthcare field have been opened and published up to the specified time.

Job Description :

DUTIES AND RESPONSIBILITIES The specific responsibilities will depend on the requirements of each team, but may include: Attend project related meetings, or teleconferences, as necessary, producing minutes in a timely manner. Assist with general preparation for audit and inspections within assigned team. Set up and initiation of allocated trials within an assigned team, under the guidance of the Senior Research Project Manager. Provide administrative support to the Principal Investigators and delegated trials team for safety reporting in accordance with protocol requirements. Maintain investigator site files and essential documentation in accordance with ICH-GCP and Trust SOPs to ensure they are kept inspection ready at all times. Complete case report forms as per sponsor requirements, and liaise with clinical trial monitors to ensure the data sent is valid and their requirements are met at site monitoring visits. Process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines. Archive all trial radiology documents following the Trusts archiving guidelines. Track all payments throughout each clinical trial including completion of activity logs and requesting invoices to be raised. Act as a point of contact for the Research and Innovation core team, external study sponsors, contract research organisations (CROs) and specific research teams, communicating directly with them regarding data queries, monitoring visits and other enquiries relevant to general trial conduct. Complete team reporting mechanisms (i.e. recruitment activity logs, patient visit logs, costing spreadsheets, case report form trackers and electronic proformas). Produce trial workbooks for review by the Principal Investigator for assigned studies and ensure version control is maintained. Cross check, confirm data and complete query resolution with sponsors and third parties in a timely manner. Completion of clinical trial specific databases with data from various sources such as questionnaires, hospital records and other electronic and paper sources. Arrange shipping and delivery of relevant trial data and documents including import/export of tumour blocks, ECGs and copy scans. Arrange team and trial related meetings as required, producing minutes in a timely manner. Ensure that data is available and up to date for any meetings related to a clinical trial. Demonstrates the agreed set of values and accountable for own attitude and behaviour. Maintain the radiology clinical trials database including accurate patient data entry, imaging, and resolution of discrepancies between Trust information systems (CRIS, CWP) for patients taking part in clinical trials associated with radiology. Produce copy scan images for research purposes ensuring GCP and GDPR requirements are followed in the production and transfer of images. Maintain tracking systems i.e. attendance and appointment stats, copy scan logs, clinical trials database maintenance in response to service needs. Contribute to continuous developments and the future development of the radiology clinical trials service.