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
- Solid 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.
📌 CRA / Senior CRA (Noida)
🏢 N Human Resources u0026 Management Systems
📍 Noida
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