Clinical Research Associate Job at The George Institute for Global Health | Apply Now
Looking for a clinical research associate job in Delhi? The George Institute for Global Health is hiring a Clinical Research Associate (CRA) for its New Delhi location. This opportunity is ideal for professionals with experience in clinical trial coordination who are seeking impactful medical jobs in Delhi. If you are passionate about global health research and want to work on large-scale international trials, this could be the right career move.
Job details:
- Job Position: Clinical Research Associate (CRA)
- Location: New Delhi
About the Company:
The George Institute for Global Health is a leading medical research institute affiliated with top universities worldwide. With more than 700 professionals working across 40+ countries, the Institute focuses on improving healthcare outcomes globally, especially for disadvantaged populations. The organisation’s Strategy 2025 focuses on impact — particularly improving the health of millions of people worldwide. Its three key research priorities include:
- Better Treatments: finding better treatments for the world’s biggest health problems
- Better Care: transforming primary health care to support better health for more people
- Healthier Societies: improving health through communities, governments, and markets
The Institute works on major global health challenges such as stroke, heart disease, high blood pressure, kidney disease, and mental health. From developing affordable dialysis machines to running large-scale awareness programs, the organisation is creating meaningful change in global health systems.
Job Description:
The Clinical Research Associate (CRA) will work on trials testing new and existing drugs. The role includes managing clinical trial operations from start to finish. The CRA will directly report to the Senior Project Manager.
Qualifications:
- Qualification in medical sciences
- Minimum 2 years of experience in clinical trial coordination.
- Willingness to travel for frequent site monitoring visits.
- Strong analytical and problem-solving skills.
- Excellent English communication skills.
- Ability to work independently and collaboratively.
- Strong organisational skills and attention to detail.
- Ability to work under pressure and adapt to changing priorities.
Key Responsibilities:
- Assist in developing trial-related documents, including protocols, investigator’s brochures, patient information documents, and case report forms (CRFs).
- Coordinate with the ethics committee to safeguard trial subjects.
- Assist in regulatory authority applications and approvals.
- Assess the suitability of facilities for clinical trial sites.
- Assist in selecting investigators responsible for conducting the trial.
- Liaise with doctors, consultants, and investigators.
- Set up trial sites and ensure availability of trial materials including investigational medicinal products (IMP).
- Train site staff according to trial-specific standards.
- Conduct regular site monitoring visits and resolve issues.
- Perform source data verification (SDV).
- Collect completed CRFs from hospitals and practices.
- Write visit reports and maintain trial documentation.
- Discuss ongoing trials, trends, and adverse events with team members.
- Ensure unused trial supplies are accounted for.
- Close trial sites and archive study documentation.
- Prepare final reports for sponsors, regulatory authorities, and ethics committees.
