A Clinical Research Associate (CRA) is a healthcare and research skilled responsible for monitoring and managing clinical trials to ensure they are conducted according to study protocols, regulatory guidelines, and ethical standards.
Role & responsibilities
Monitor clinical trial sites and ensure compliance with protocols, Positive Clinical Practice (GCP), and regulatory requirements.
Review study documents, source data, and case report forms (CRFs).
Conduct site initiation, monitoring, and close-out visits.
Verify the accuracy and completeness of clinical data collected during the study.
Ensure patient safety and proper reporting of adverse events.
Coordinate with investigators, study coordinators, sponsors, and other stakeholders.
Maintain trial documentation and prepare monitoring reports.
Support audit and inspection readiness throughout the study.
📌 Clinical Research Associate Hyderabad
🏢 Proxima Skills Training Consulting Services
📍 Hyderabad
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