Job Description

Study Coordination:

Assist in the design and development of study protocols and case report forms (CRFs) Coordinate the logistics of clinical trials or medical research projects Manage timelines, budgets, and resources for research studies

Site & Data Management:

Support site selection and initiation Monitor clinical trial sites to ensure compliance with protocols and regulations Collect, review, and verify study data for accuracy and completeness Maintain regulatory documentation and study master files

Regulatory & Ethical Compliance:

Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and applicable laws (e.g., CDSCO in India, FDA in the US) Assist in ethics committee/institutional review board (IRB) submissions and communications Support preparation of study reports and submissions to regulatory authorities
Job Type: Full-time

Pay: From ?10,000.00 per month

Schedule:

Day shift
Supplemental Pay:

Performance bonus
Work Location: In person