We are seeking an organized and compassionate Clinical Trial Coordinator to join our on-site research team. In this role, you will champion patient safety and data integrity while executing clinical trial protocols from screening to study closure. You will work closely with the Principal Investigator (PI) to manage patient visits, collect critical study data, and ensure seamless daily operations.

Key Responsibilities - Duration : 3-4 Months

Patient Screening & Recruitment

• Pre-screen potential participants by reviewing medical charts and histories to assess preliminary eligibility against protocol-specific inclusion/exclusion criteria.
• Coordinate and conduct the informed consent process, ensuring patients fully understand the study's requirements, risks, and benefits.
• Schedule and manage screening visits, working with the PI to confirm final eligibility before enrollment.

Patient Visits &...