Clinical Research Coordinator

About the Role

We are seeking a Clinical Research Coordinator to support the conduct of Phase II and III clinical trials at a NABH-accredited research site in Bengaluru. You will be responsible for ensuring that trials are executed in compliance with GCP, ICH guidelines, and the study protocol. This is a critical role that directly supports the timely delivery of clinical data and, ultimately, the approval of new therapies.

Key Responsibilities

• Coordinate daily activities for clinical trials in compliance with study protocols and GCP.
• Recruit, screen, and enrol eligible subjects for ongoing studies.
• Ensure accurate and timely data collection and CRF completion.
• Maintain essential trial documents and investigator site files (ISF).
• Assist with ethics committee submissions and facilitate monitoring visits.

Requirements & Experience

• 2-5 years of experience coordinating clinical trials.
• Degree in Life Sciences, Nursing, or related field; Clinical Research certification preferred.
• In-depth knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Experience with EDC (Electronic Data Capture) systems.
• Strong organisational skills and ability to manage multiple trials simultaneously.