Research Coordinator

Role & responsibilities

• Participant Management: Recruit, screen, and enroll study candidates while explaining procedures and securing informed consent.
• Regulatory Compliance: Prepare and submit documents to Institutional Review Boards (IRBs) and ensure the study follows strict ethical and legal rules.
• Data Collection: Gather, enter, and monitor study data to maintain high accuracy and quality control.
• Study Operations: Schedule participant visits, manage project timelines, and organize supplies or lab samples.
• Communication: Act as the primary contact point for sponsors, medical staff, and the research team.

Preferred candidate profile

• Qualification: M.Sc. (relevant scientific/medical discipline)
• Experience: 2 to 5 years of experience in a medical college or clinical research setting