Clinical Research Associate Full-time Job

The Clinical Research Associate (CRA) manages clinical trials to ensure they are conducted according to regulatory requirements and study protocols. Responsibilities include site selection, initiation, monitoring, and closure. You will work closely with investigators to facilitate patient recruitment and ensure compliance with Good Clinical Practice (GCP). The CRA is responsible for data collection, ensuring data accuracy, and preparing reports for regulatory submissions. Regular visits to clinical trial sites are required to monitor trial progress and address any issues. The role demands strong organizational and communication skills, as well as the ability to work independently and manage multiple tasks.