Assist in setting up, monitoring, and closing clinical trial sites under supervision.
Ensure trials are conducted in compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
Perform site visits (remote or on-site) and assist with source data verification.
Maintain study documentation and track essential documents.
Support the collection, review, and submission of trial-related documentation (e.g., informed consent forms, CRFs).
Assist with training site staff on study protocols and procedures.
Collaborate with cross-functional teams, including project managers, data managers, and regulatory staff.
Report any deviations, issues, or safety concerns to the study lead.
Participate in internal training programs to gain knowledge of clinical trial processes.
Job Types: Full-time, Fresher
Pay: ₹22,800.49 - ₹38,652.15 per month
Benefits:
Health insurance
Paid sick time
Paid time off
Work Location: In person
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