· Organizing and maintaining trial documentation, coordinating study visits, and managing regulatory binders.
· Assisting in enrolling participants and ensuring compliance with trial protocols.
· Collecting, entering, and maintaining trial data while ensuring accuracy.
· Assisting with ethics submissions, site initiation, and adherence to Good Clinical Practice (GCP) guidelines.
· Assisting with ethics submissions, site initiation, and adherence to Good Clinical Practice (GCP) guidelines.
· Managing trial supplies, scheduling meetings, and ensuring smooth operations.
Job Types: Part-time, Contractual / Temporary
Pay: ₹12,000.00 - ₹18,000.00 per month
Work Location: In person
