The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.
While projects vary, your typical responsibilities might include:
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentationSupporting the development of a subject recruitment planEstablishing regular lines of communication plus administering protocol and related study training to assigned sitesEvaluating the quality and integrity of site practices – escalating quality issues as appropriateManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionYou will need to b...