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

• Valuable understanding of ICH-GCP and regulatory requirements

Interested candidates can share their updated resume.

📌 CRA / Senior CRA (Noida)
🏢 N Human Resources & Management Systems
📍 Noida