Job description
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.