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.