(CRC) is responsible for the day-to-day coordination and management of clinical research studies in compliance with regulatory requirements, study protocols, and institutional policies. The CRC serves as a key liaison among investigators, study participants, sponsors, and regulatory bodies to ensure high-quality data collection and participant safety.
Key Responsibilities:
Coordinate clinical trial activities in compliance with ICH-GCP guidelines, study protocols, and applicable regulatory requirements
Maintain accurate and complete site documentation, ensuring ongoing adherence to protocol, regulatory, and institutional standards
Assist with patient screening, recruitment, enrollment, and follow-up activities in accordance with study requirements
Support site monitoring visits, audits, and inspections, ensuring continuous audit readiness
Facilitate effective communication and collaboration with investigators, sponsors, CROs, and regulatory stakeholders
Job Types: Full-time, Permanent
Pay: ₹18,000.00 - ₹24,000.00 per month
Work Location: In person
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