Job Description

Assist in the preparation and coordination of clinical trial protocols and associated documents. Support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close-out. Ensure that study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements. Conduct site visits to assess the progress of clinical trials, monitor data accuracy, and ensure patient safety. Communicate with investigators and site staff to address issues or concerns related to the clinical trials. Assist in the review and management of clinical trial documentation, including case report forms (CRFs), informed consent forms, and regulatory submissions. Maintain study files and data to ensure compliance with applicable regulatory agencies. Support the clinical team in preparing reports, including monitoring reports and other regulatory documents. Attend and participate in internal meetings, as well as relevant training sessions, to develop knowledge and skills in clinical research.
Job Types: Full-time, Fresher

Pay: ₹22,869.01 - ₹38,019.71 per month

Benefits:

Health insurance Paid sick time Provident Fund
Work Location: In person