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 exp...