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

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