India's DMPLOI - Jobs & Networking AppIQVIA, a global leader in clinical research, healthcare analytics, and life sciences solutions, is inviting applications for the position of Clinical Data Management Professional. This opportunity is ideal for experienced professionals with a background in Life Sciences, Pharmacy, or Biotechnology who want to contribute to global clinical trials and healthcare innovation.
The role offers exposure to advanced clinical data platforms, international studies, and a collaborative work environment while ensuring the highest standards of data quality and regulatory compliance.
Job Overview
Particulars Details
Company Name
IQVIA
Position
Clinical Data Management Professional
Industry
Clinical Research, Healthcare & Life Sciences
Job Type
Full-Time
Work Mode
Hybrid
Experience Required
2–5 Years
Educational Qualification
Life Sciences / Pharmacy / Biotechnology
Salary Range
₹6 LPA – ₹12 LPA
Job Locations
Kochi, Kolkata, Thane, Hyderabad, Bangalore, Pune
Salary may vary based on experience, skills, and interview performance.
About IQVIA
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services for the healthcare industry. The company supports pharmaceutical, biotechnology, and medical device organizations in accelerating innovation and improving patient outcomes worldwide.
Key Responsibilities
Selected candidates will be responsible for:
Managing end-to-end Clinical Data Management (CDM) activities.
Supporting study startup, conduct, and closeout activities.
Configuring and managing studies using Medidata Rave EDC.
Performing clinical data review and validation.
Reviewing, cleaning, and reconciling clinical trial data.
Managing and resolving clinical database queries.
Supporting issue resolution and database lock activities.
Collaborating with sponsors and cross-functional stakeholders.
Ensuring data quality and regulatory compliance.
Supporting global clinical trial data management processes.
Required Skills
Candidates should possess knowledge and experience in:
Clinical Data Management (CDM)
Medidata Rave EDC
Clinical Trial Data Review
Query Management
Data Cleaning & Validation
Database Lock Activities
Clinical Study Lifecycle Management
ICH-GCP Guidelines
Analytical Thinking & Problem Solving
Effective Communication Skills
Experience Requirements
Applicants should have:
2–5 years of core Clinical Data Management experience.
Hands-on experience with Medidata Rave EDC.
Study Startup experience.
Study Conduct experience.
Study Closeout experience.
Clinical Trial Data Review and Query Management expertise.
Why Join IQVIA?
Global Exposure
Work on international clinical studies and collaborate with global healthcare professionals.
Career Growth
Access structured learning programs, certifications, and professional development opportunities.
Advanced Technology
Gain experience with cutting-edge clinical data management platforms and tools.
Collaborative Culture
Work alongside talented professionals in a diverse and inclusive environment.
Competitive Benefits
Receive industry-standard compensation and attractive employee benefits.
Employee Benefits
Hybrid Work Environment
Global Clinical Trial Exposure
Professional Development Programs
Advanced CDM Technology Experience
Learning & Certification Opportunities
Cross-Functional Team Collaboration
Career Growth Opportunities
Competitive Compensation & Benefits
Salary Details
The expected salary range for this role is ₹6 LPA to ₹12 LPA, depending on:
Experience level
Technical expertise
Domain knowledge
Interview performance
Relevant certifications
How to Apply?
Interested candidates can share their updated resume to:
Email: vaishnavinandkishor.kamble@iqvia.com
Subject Line: Clinical Data Management Professional Application
Candidates are advised to update their CV with relevant Clinical Data Management, Medidata Rave EDC, and Clinical Trial experience before applying.
Technical FAQs
1. What is Clinical Data Management (CDM) in clinical research?
Clinical Data Management is the process of collecting, validating, cleaning, and managing data generated during clinical trials to ensure accuracy, consistency, and compliance with regulatory requirements.
2. What is Medidata Rave EDC and why is it important?
Medidata Rave EDC is an Electronic Data Capture platform used to collect and manage clinical trial data. It helps streamline data entry, validation, query management, and regulatory compliance.
3. What are database lock activities in clinical trials?
Database lock is the final process where all clinical data is reviewed, cleaned, and approved before statistical analysis. Once locked, no further modifications can be made without formal procedures.
4. What is query management in Clinical Data Management?
Query management involves identifying discrepancies or missing information in clinical trial data and coordinating with study sites to resolve issues while maintaining data integrity.
5. Why is ICH-GCP knowledge essential for Clinical Data Managers?
ICH-GCP (International Council for Harmonisation – Good Clinical Practice) provides global standards for designing, conducting, recording, and reporting clinical trials, ensuring participant safety and data credibility.
Conclusion
The IQVIA Clinical Data Management Professional Hiring 2026 opportunity is an excellent career move for Life Sciences, Pharmacy, and Biotechnology professionals with 2–5 years of Clinical Data Management experience. With competitive salaries, hybrid work flexibility, global project exposure, and advanced technology platforms, IQVIA offers a strong platform for long-term career growth in the clinical research industry. Interested candidates should apply as soon as possible and take the next step in their Clinical Data Management career.
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