Key Responsibilities:
Assist clinical project managers in planning and executing clinical trials
Support project tracking, timelines, and deliverables
Maintain and update project documentation and Trial Master File (TMF)
Coordinate with cross-functional teams including CRAs, data management, and regulatory teams
Prepare project status reports and dashboards
Support study start-up, conduct, and close-out activities
Ensure compliance with protocols, SOPs, GCP, and regulatory guidelines
Assist in organizing meetings, preparing agendas, and documenting minutes
Eligibility Criteria:
Educational Qualification:
B.Pharm / M.Pharm
B.Sc / M.Sc (Life Sciences, Biotechnology, Microbiology, Biochemistry, etc.)
Any Life Science-related degree
Pay: ₹250,000.00 - ₹370,000.00 per year
Perks:
Health insurance
Paid sick time
Provident Fund