Job Description

Assist in monitoring clinical trials at investigational sites under supervision Ensure compliance with ICH-GCP guidelines, regulatory requirements, and company SOPs Support site initiation, routine monitoring, and close-out visits Help in verifying source data and case report forms (CRFs) Maintain study documentation and track trial progress Assist in identifying and resolving site issues and deviations Coordinate with investigators, site staff, and internal study team Participate in training programs and development activities Prepare visit reports and documentation under supervision Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field
Job Types: Full-time, Permanent, Fresher

Pay: ₹23,858.48 - ₹38,990.58 per month

Benefits:

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