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: 35 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.
MBA- HR or relevant Experience in Hospital Industry.
4-5 yea...