Looking to step up your career in Clinical Data Management (CDM)? IQVIA, one of the world’s leading clinical research and technology-driven healthcare companies, is hiring skilled CDM professionals with 3+ years of core industry experience. If you are passionate about transforming clinical data into meaningful insights and enjoy working with Medidata Rave, this opportunity is tailor-made for you.
This article covers job roles, responsibilities, eligibility, benefits, locations, and how to apply, optimized for search visibility across Google Discover and AI Overviews.
⭐ About the Role
IQVIA is expanding its global CDM team and seeking experienced professionals to support clinical study lifecycle activities, including study start-up, conduct, and database lock.
🧪 Key Responsibilities
- Manage end-to-end Clinical Data Management activities across study lifecycle
- Execute User Acceptance Testing (UAT), validation checks & query management
- Perform SAE, Lab & Third-Party Vendor (TPV) data reconciliation
- Ensure timely database lock with high accuracy
- Collaborate with cross-functional teams ensuring data quality & regulatory compliance
- Maintain documentation as per global CDM standards
🎓 Required Qualifications
- Minimum 3+ years of experience in Core Clinical Data Management
- Hands-on experience with Medidata Rave
- Strong understanding of clinical study lifecycle and CDM best practices
- Ability to work in shift-based & hybrid model
- Excellent communication and problem-solving skills
🌍 Job Locations
Hiring for multiple cities across India:
- Kochi
- Kolkata
- Bangalore
- Thane
Work Mode: Hybrid
Shift Flexibility: Required
💼 Why Join IQVIA?
- Work on global, high-impact clinical trials
- Collaborative and innovation-driven workplace
- Competitive salary & comprehensive employee benefits
- Opportunity to upscale skills in advanced CDM platforms like Rave
📩 How to Apply
Send your updated CV directly to:
Email: jinto.jacobc@iqvia.com
