The George Institute Clinical Research Associate (CRA) job in New Delhi is an excellent opportunity for experienced clinical research professionals seeking to work on large-scale global trials in non-communicable diseases (NCDs).
The George Institute for Global Health is a globally recognized medical research organization affiliated with leading universities. With operations in 40+ countries and over 700 researchers worldwide, the institute focuses on improving global health outcomes, particularly in cardiovascular, renal, and chronic diseases.
If you have at least 2 years of clinical trial coordination experience and are looking to advance your career as a Clinical Research Associate in Delhi, this could be the right move.
📌 Job Overview
- Job Title: Clinical Research Associate (CRA)
- Location: New Delhi
- Employment Type: Two-year contract (extendable)
- Department: Projects
- Career Level: Intermediate
- Reporting To: Senior Project Manager
This Clinical Research Associate job involves managing multi-site clinical trials, regulatory coordination, ethics submissions, site monitoring, and ensuring compliance with ICH-GCP standards.
🔬 Key Responsibilities – Clinical Research Associate
The CRA role at George Institute includes end-to-end clinical trial management responsibilities:
Clinical Trial Start-Up
- Assist in protocol, Investigator’s Brochure, CRF, and patient information document preparation
- Coordinate with Ethics Committees and Regulatory Authorities
- Conduct site feasibility assessments
- Support investigator selection and site initiation
Trial Monitoring & Execution
- Perform frequent on-site monitoring visits
- Conduct Source Data Verification (SDV)
- Ensure CRF accuracy and regulatory compliance
- Train site staff on trial-specific procedures
- Manage Investigational Medicinal Product (IMP) accountability
Documentation & Close-Out
- Prepare monitoring visit reports
- Archive trial documentation
- Prepare final reports for sponsors and regulatory authorities
- Close trial sites upon study completion
This role demands strong clinical operations expertise, regulatory understanding, and stakeholder coordination skills.
🎓 Qualifications & Experience Required
To apply for this Clinical Research Associate job in Delhi, candidates must have:
- Qualification in Life Sciences, Medical Sciences, or Nursing
- Minimum 2 years of clinical trial coordination experience
- Strong knowledge of:
- ICH-GCP guidelines
- Ethics Committee submissions
- Regulatory approvals
- Clinical documentation and CRF handling
- Willingness to travel for site monitoring visits
- Excellent English communication skills
Professionals with experience in NCD trials, cardiovascular research, or renal studies will have an added advantage.
🌍 Why Join George Institute?
Working as a Clinical Research Associate at George Institute offers:
- Exposure to multi-country clinical trials
- Opportunity to work on impactful NCD research
- Career growth in global clinical research operations
- Collaborative and inclusive work environment
- Performance-based contract extension
The organization actively promotes diversity, inclusion, and ethical research standards.
💰 Salary (Estimated)
Based on similar Clinical Research Associate jobs in Delhi:
- Estimated Salary Range: ₹5,00,000 – ₹8,50,000 per annum (depending on experience)
📅 Application Process
Interested candidates should:
- Email updated resume with:
- Current CTC
- Expected CTC
- Notice period
- Mention subject line: Clinical Research Associate (CRA)
- Send to: hrindia@georgeinstitute.org.in
