3 - 8 years
0 Lacs
Posted:1 month ago|
Platform:
On-site
Full Time
A Clinical Research Associate (CRA) is responsible for
overseeing and coordinating clinical trials to ensure they are conducted safely and effectively, monitoring data collection, ensuring regulatory compliance, and serving as a liaison between study sites, sponsors, and regulatory agencies. Key duties include setting up trials, managing trial supplies, verifying data accuracy, and preparing reports. Core responsibilities Trial management: Plan, set up, and manage all stages of a clinical trial, from site selection to closing out the study. Oversight and monitoring: Monitor the trial's execution to ensure it follows the protocol and complies with Good Clinical Practice (GCP) guidelines. Data integrity: Collect, verify, and manage data to ensure its accuracy and quality. Site communication: Act as a liaison between the clinical trial sites and the sponsor, ensuring smooth communication and resolving issues. Regulatory compliance: Ensure all aspects of the trial adhere to relevant regulations and ethical guidelines. Typical duties Conduct site visits to monitor the progress of the trial. Verify source data and review trial-related documents, such as informed consent forms. Manage trial supplies and drug accountability. Ensure participant safety throughout the trial. Assist in preparing post-trial reports and publications.
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