Looking to step up your career in Clinical Data Management (CDM)? IQVIA, one of the worldโs 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.
โญ 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.
๐งช 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
๐ 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
๐ Job Locations
Hiring for multiple cities across India:
- Kochi
- Kolkata
- Bangalore
- Thane
Work Mode: Hybrid
Shift Flexibility: Required
๐ผ 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
๐ฉ How to Apply
Send your updated CV directly to:
Email: jinto.jacobc@iqvia.com
