Looking to build a strong career in clinical research jobs in India? IQVIA is hiring Clinical Research Associate I (CRA I) for Bangalore and Mumbai locations.
This is a high-demand role for candidates aiming to enter or grow in CRA jobs, clinical trial monitoring, and GCP-compliant research environments. If you have a background in life sciences and want hands-on exposure to site monitoring, TMF, ISF, and clinical trial operations, this opportunity is highly valuable.
Job Overview – Clinical Research Associate I
The CRA I will be responsible for site monitoring and clinical trial management, ensuring compliance with ICH-GCP guidelines, protocol adherence, and regulatory standards.
This role is critical in ensuring data integrity, patient safety, and successful clinical trial execution.
Key Responsibilities (CRA I – IQVIA)
- Perform site monitoring visits (SIV, IMV, COV) as per ICH-GCP guidelines
- Manage clinical trial sites and ensure protocol compliance
- Track subject recruitment and enrollment strategies
- Conduct site training and communication with investigators
- Ensure proper maintenance of:
- Trial Master File (TMF)
- Investigator Site File (ISF)
- Review CRFs (Case Report Forms) for completeness and accuracy
- Handle data queries and resolution processes
- Submit monitoring visit reports and follow-up letters
- Support study start-up activities and regulatory submissions
- Coordinate with cross-functional teams for clinical trial execution
- Manage site financial tracking and invoices (if applicable)
Eligibility & Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or Healthcare
- Strong understanding of:
- ICH-GCP guidelines
- Clinical trial processes
- Good knowledge of protocols and therapeutic areas
- Skills required:
- Communication & stakeholder management
- Problem-solving & organization
- Time & financial management
- Technical skills:
- MS Word, Excel, PowerPoint
- Clinical systems exposure (preferred)
Why This CRA Role is Important
This position gives exposure to:
- Real-world clinical trial monitoring
- Hands-on site management experience
- Direct involvement in patient safety & regulatory compliance
- Career progression path:
- CRA I → CRA II → Senior CRA → Project Manager
Salary & Benefits (Estimated)
- 💰 Salary Range: ₹5,00,000 – ₹8,50,000 per annum
- 📈 Career growth in top global CRO
- 🌍 Exposure to international clinical trials
- 📚 Training in GCP, monitoring, and regulatory compliance
- 🤝 Collaborative global work environment
Job Location
- Bangalore, India
- Mumbai, Maharashtra, India
How to Apply
