Assist in monitoring clinical trial sites to ensure adherence to study protocols, SOPs, and regulatory guidelines.
Support in reviewing essential clinical trial documents such as informed consent forms, case report forms (CRFs), and investigator site files.
Participate in site initiation, routine monitoring, and close-out visits under supervision.
Ensure accurate and timely data collection, entry, and reporting.
Assist in identifying, resolving, and documenting protocol deviations and data discrepancies.
Maintain effective communication with investigators, site staff, and project teams.
Support the preparation of trial-related reports and regulatory submissions.
Ensure trial-related documentation is complete and up to date.
Job Types: Full-time, Permanent, Fresher
Pay: ₹226,488.77 - ₹538,976.46 per year
Benefits:
Health insurance
Paid sick time
Work Location: In person
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