Clinical Monitoring Associate

IQVIA''s Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.The Clinical Research Associate will support Oncology studies and cover sites across the UKApply today and forge a career with greater purpose, make an impact and never stop learning!ResponsibilitiesPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator''s Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.Create and maintain appropriate documentation ..... full job details .....