CRA / Senior CRA

N Human Resources & Management Systems; Dadri; On-site; INR 600,000 - 800,000; Full time

Job summary

N Human Resources & Management Systems is hiring for the position of CRA / Senior CRA in Noida. We are seeking experienced Clinical Research Associates to join our growing Clinical Affairs team. The role involves handling clinical trials, coordinating with CROs, and managing regulatory documentation.

Ideal candidates should have 3–5 years of experience in clinical research, a solid understanding of ICH-GCP guidelines, and excellent site management skills. Interested candidates can share their updated resumes.

Qualifications

• 3–5 years of Clinical Research experience.
• Strong experience in Clinical Trial Handling.
• Hands-on exposure to CRO Management.

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.

Skills

Clinical Research experience

Clinical Trial Handling

CRO Management

Ethics Committee submissions

ICH-GCP knowledge

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.