Coordinate and monitor clinical research studies as per approved protocols
Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements
Assist in site initiation, monitoring, and close-out activities
Verify accuracy, completeness, and consistency of clinical trial data
Maintain essential documents (TMF, investigator files, CRFs, consent forms, etc.)
Conduct source data verification (SDV) and ensure data integrity
Report deviations, adverse events, and safety issues timely
Liaise with investigators, project teams, and internal stakeholders
Support audits, inspections, and regulatory submissions
Prepare monitoring reports and study-related documentation
Bachelor’s / Master’s degree in Life Sciences, Pharmacy, Nursing, or related field
Fresher or 1–3 years of experience in clinical research (NGO or healthcare projects preferred)
Knowledge of ICH-GCP guidelines and clinical trial processes
Good understanding of clinical documentation and regulatory compliance