We are looking for experienced Clinical Research Associates to join a growing Clinical Affairs team.
Key Responsibilities
Clinical trial handling and site management
CRO coordination and monitoring activities
Ethics Committee submissions and regulatory documentation
Site initiation, monitoring, and close-out activities
Training site staff on protocols and GCP requirements
Subject safety and compliance management
Investigational Product accountability and reconciliation
Preparation of monitoring reports and study documentation
Ensuring compliance with ICH-GCP guidelines and SOPs
Requirements
3–5 years of Clinical Research experience
Solid experience in Clinical Trial Handling
Hands-on exposure to CRO Management
Experience in Ethics Committee submissions
Positive understanding of ICH-GCP and regulatory requirements
Interested candidates can share their updated resume.
📌 Cra / Senior Cra Noida (India)
🏢 N Human Resources u0026 Management Systems
📍 India
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