Job

• The Research Associate will handle day-to-day execution of a multicentric clinical trial in accordance with the approved protocol, SOPs, and ethical guidelines.


• The RA will manage all trial documentation, including CRFs, consent forms, logs, AE/SAE reports, and protocol deviation records, and ensure compliance with GCP, ICMR, Ministry of AYUSH, and ethics committee requirements. The role includes supporting ethics submissions, progress reports, and final study documentation.


• The RA will coordinate with research teams across participating centres to ensure uniform protocol implementation, data consistency, and effective communication, and support investigator meetings and monitoring visits. Additional responsibilities include data entry, verification, quality assurance, audit support, patient safety monitoring, timely AE/SAE reporting, and assisting the PI and Co-PIs with study updates, analyses, publications, and related project activities.

acara@ay.amrita.edu