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 Type: Full-time
Pay: ?14,000.00 - ?18,000.00 per month
Schedule:
Day shift
Morning shift
Weekend availability
Work Location: In person
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