- Study Management: Oversee daily operations of multiple clinical trials, maintaining regulatory binders, and ensuring adherence to study protocols, SOPs, and guidelines.
- Participant Management: Identify, recruit, and screen potential subjects; conduct informed consent; and arrange study visits, ensuring participant safety
- Clinical Procedures: Perform study-specific tasks such as taking vitals, collecting and processing laboratory specimens (e.g., blood, samples), and performing ECGs.
- Data Management: Accurately collect and enter patient data into case report forms (CRFs) or web-based systems; respond to data queries promptly.
- Regulatory Compliance: Prepare submissions and ensure all research documents are up-to-date
- Collaboration: Coordinate with Principal Investigators (PIs), sponsors, CROs, and pharmacy for study medication distribution and monitor visits
Job Type: Full-time
Pay: Up to ₹32,000.00 per month
Benefits:
- Health insurance
- Leave encashment
- Paid sick time
- Provident Fund
Work Location: In person
