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IQVIA, a global leader in clinical research, advanced analytics, and healthcare intelligence, is hiring Clinical Data Management (CDM) professionals to join our team of over 86,000 employees across 100+ countries.
With our cutting-edge technologies and unparalleled data, we drive healthcare innovation. Explore rewarding CDM career opportunities in Bangalore, Thane, Kochi, Kolkata, and Pune, and contribute to life-changing clinical research.
Why Choose IQVIA for Clinical Data Management?
IQVIA’s mission is to improve patient outcomes through intelligent data connections and innovative solutions. Our CDM professionals play a critical role in ensuring data accuracy and compliance in clinical trials.
With a collaborative environment, advanced tools like Medidata Rave EDC, and opportunities for growth, IQVIA is the ideal place to advance your career in clinical research.
Open Clinical Data Management Positions
IQVIA is seeking skilled CDM professionals for roles in Bangalore, Thane, Kochi, Kolkata, and Pune. Below are the key details of the opportunities available.
| Role | Location | Qualification | Experience | Key Responsibilities |
|---|---|---|---|---|
| Clinical Data Specialist | Bangalore, Thane, Pune | Bachelor’s in Life Sciences, Pharmacy, or related field | 2.5+ years in CDM | Manage study startup, execution, closeout, data reconciliation, and database lock using Rave EDC |
| Clinical Data Coordinator | Kochi, Kolkata | Bachelor’s in Life Sciences or related field | 1+ year in CDM | Handle data cleaning, discrepancy management, eCRF design, and audit readiness |
Job Responsibilities
Clinical Data Specialist
- Role Overview: Lead end-to-end data management for clinical trials, ensuring quality and compliance.
- Key Responsibilities:
- Oversee study startup, conduct, and closeout activities.
- Perform data reconciliation, query management, and database lock.
- Utilize Medidata Rave EDC for data collection and reporting.
- Conduct User Acceptance Testing (UAT) for system validation.
- Ensure compliance with ICH-GCP, CDISC, and FDA guidelines.
- Who Should Apply: Professionals with 2.5+ years of CDM experience and Rave EDC proficiency.
Clinical Data Coordinator
- Role Overview: Support clinical trial data management with a focus on accuracy and efficiency.
- Key Responsibilities:
- Manage data cleaning, discrepancy resolution, and validation.
- Support eCRF design and database testing.
- Collaborate with CRAs, biostatisticians, and sponsors.
- Ensure audit readiness and compliance with regulatory standards.
- Who Should Apply: Candidates with 1+ year of core CDM experience and knowledge of clinical trial phases.
Required Skills and Qualifications
To excel in these roles, candidates should possess:
- Education: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields.
- Experience: 1-5 years in Clinical Data Management (role-dependent).
- Technical Skills: Proficiency in Medidata Rave EDC, Oracle Clinical, or Veeva systems.
- Soft Skills:
- Strong analytical and problem-solving abilities.
- Excellent communication and teamwork skills.
- High attention to detail and organizational capabilities.
- Preferred: Certification in Clinical Data Management (not mandatory).
Why Work at IQVIA?
- Global Impact: Contribute to clinical research that improves patient outcomes worldwide.
- Career Growth: Access training, certifications, and an AI-powered talent marketplace for career advancement.
- Innovative Environment: Work with cutting-edge technologies like the IQVIA Human Data Science Cloud.
- Benefits: Competitive salaries, shift allowances, health insurance, and flexible work options.
How to Apply
Create a profile on IQVIA’s career page to receive alerts for new CDM opportunities matching your skills. Upload your resume, including your first name, last name, email, country, and area of interest (Clinical Data Management). Specify your current CTC, expected CTC, and notice period. Alternatively, email your CV to jinto.jacobc@iqvia.com for roles in Bangalore, Thane, or Pune.
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Why Clinical Data Management at IQVIA?
Clinical Data Management is a high-demand field with a projected market growth of 13.2% CAGR from 2023 to 2031. At IQVIA, you’ll work on impactful clinical trials, leveraging advanced analytics and global expertise to ensure data integrity. Our shift-based roles offer flexibility, making it a rewarding career for Life Sciences professionals.
Benefits of Joining IQVIA
- Professional Development: Access to in-house training and global conferences.
- Work-Life Balance: Flexible policies and remote/hybrid work options.
- Collaborative Culture: Work with global teams and industry experts.
- Health and Wellness: Comprehensive health insurance and wellness programs.
Take the Next Step in Your CDM Career
Join IQVIA to drive healthcare forward through clinical data management. Create your profile on IQVIA’s career page or email your CV to jinto.jacobc@iqvia.com. For more insights into clinical research careers, explore IQVIA’s career resources