Clinical Research Coordinator

Participant Management: Develop recruitment strategies to identify and enroll eligible participants. Screen potential participants against study inclusion and exclusion criteria. Administer informed consent to explain study procedures, risks, and benefits. Monitor participant health, collect data, and manage any adverse events. Study Operations: Coordinate and conduct all day-to-day activities for the clinical trial. Ensure strict adherence to the study protocol, regulatory guidelines, and Institutional Review Board (IRB) requirements. Collect, process, and ship laboratory specimens. Manage study supplies and equipment. Documentation and Data Management: Maintain comprehensive and organized research documentation, including consent forms, case report forms, and adverse event reports. Collect, manage, and enter accurate study data into databases. Assist with budget preparation and financial tracking for the study. Assist in writing research proposals, reports, and manuscripts.

Job Types: Full-time, Part-time, Fresher

Pay: ₹26,000.00 - ₹38,275.09 per month

Benefits:

• Provident Fund

Work Location: In person