Job Description
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities include conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process, while collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data and contributing to the preparation and review of study documentation, including protocols and clinical study reports.
About iCIMS
iCIMS is a software company that provides a recruiting platform that enables companies to manage their entire talent acquisition lifecycle.