Posted:19 hours ago|
Platform:
On-site
Full Time
· 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
Work Location: In person
NovoBliss Research Pvt Ltd
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