Key Responsibilities 1 Study Monitoring Conduct site initiation routine monitoring and close-out visits Ensure adherence to study protocol GCP guidelines regulatory requirements Verify informed consent forms and ensure ethical compliance Review and validate source documents CRFs and eCRF entries Identify protocol deviations and ensure corrective actions are implemented 2 Site Management Train investigators coordinators and site staff on study procedures Maintain oversight of site performance and subject recruitment status Ensure availability of study supplies trial materials and drug accountability Build robust relationships with investigators and site teams 3 Documentation Compliance Maintain Trial Master File TMF and site-level documentation Ensure timely reporting of adverse events AEs and serious adverse events SAEs Prepare monitoring reports and follow-up letters Ensure data integrity and compliance with SOPs ICH-GCP CDSCO EMA FDA requirements 4 Coordination Communication Work with project managers data managers and medical monitors Participate in investigator meetings and internal team meetings Provide feedback and updates on site status and trial progress Job Type Full-time Pay 30 000 00 - 40 000 00 per month Benefits Health insurance Provident Fund Work Location In person

📌 Clinical Research Associate (New Delhi)
🏢 AURIGA RESEARCH
📍 New Delhi