CRA / Senior CRA

Hiring: CRA / Senior CRA ? Location: Noida 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
• Strong experience in Clinical Trial Handling
• Hands-on exposure to CRO Management
• Experience in Ethics Committee submissions
• Good understanding of ICH-GCP and regulatory requirements Interested candidates can share their updated resume.