Support clinical research teams with trial documentation and coordination.
Maintain accurate and up-to-date study files and records.
Assist with the preparation and organization of trial documentation.
Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
Skills
:
Strong organizational and time-management skills
Excellent verbal and written communication abilities
Proficiency in Microsoft Office tools
Job Type: Full-time
Pay: ₹18,000.00 - ₹45,000.00 per month
Benefits:
Health insurance
Provident Fund
Work Location: In person
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