IQVIA, a global leader in clinical research, healthcare analytics, and technology-enabled services, is expanding its Clinical Data Management (CDM) team in India. The company is hiring Associate Clinical Data Coordinators and Clinical Data Specialists across multiple locations for professionals with 1–6 years of Clinical Data Management experience.

If you have experience in Medidata Rave, EDC systems, clinical trial data review, query management, database lock, and study conduct, this is an excellent opportunity to grow your career with one of the world’s leading clinical research organizations.

IQVIA Clinical Data Management Recruitment 2026 – Overview

Job Responsibilities

Selected candidates will support clinical studies by ensuring high-quality clinical trial data throughout the study lifecycle.

Responsibilities include:

• Perform clinical study setup activities.
• Configure and support Electronic Data Capture (EDC) systems.
• Review, clean, and validate clinical trial data.
• Perform clinical data review and discrepancy management.
• Generate, review, and resolve data queries.
• Support study conduct activities throughout clinical trials.
• Participate in database lock and study closeout.
• Maintain compliance with ICH-GCP, SOPs, and regulatory guidelines.
• Ensure data integrity, quality, consistency, and completeness.
• Collaborate with cross-functional global clinical study teams.

Eligibility Criteria

Associate Clinical Data Coordinator

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Medicine, or related healthcare discipline.
• 1–2 years of Clinical Data Management experience.
• Basic understanding of clinical trials and EDC systems.
• Good analytical, communication, and problem-solving skills.

Clinical Data Specialist

• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Nursing, Medicine, Clinical Research, or related field.
• 2–6 years of Clinical Data Management experience.
• Hands-on experience with Medidata Rave (EDC).
• Experience in:
  • Study Set-Up
  • Study Conduct
  • Database Lock
  • Study Closeout
• Ability to work in collaborative and shift-based environments.

Who Can Apply?

Suitable qualifications include:

B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc (Life Sciences/Biotechnology/Microbiology/Biochemistry), B.Tech Biotechnology, M.Tech Biotechnology, BDS, MBBS, BAMS, BHMS, BPT, Nursing (B.Sc/GNM), MSc Clinical Research or other relevant Life Science qualifications with Clinical Data Management experience.

Preferred Skills

• Clinical Data Management
• Medidata Rave
• Electronic Data Capture (EDC)
• Clinical Trials
• Query Management
• Database Lock
• Data Validation
• Clinical Data Review
• Study Set-Up
• Study Conduct
• Good Documentation Practices
• ICH-GCP
• Regulatory Compliance
• Problem Solving
• Communication Skills

Work Location

Hybrid opportunities are available in:

• Thane
• Pune
• Bengaluru
• Hyderabad
• Kochi
• Kolkata

Why Join IQVIA?

IQVIA offers an excellent career path for Clinical Data Management professionals.

Benefits include:

• Global clinical research exposure
• Hybrid working model
• Competitive salary packages
• Career development programs
• Continuous learning opportunities
• Inclusive work culture
• Opportunity to contribute to life-changing clinical research
• International project exposure

Salary

Based on current market trends for similar IQVIA Clinical Data Management roles:

Estimated Salary: ₹5.5 LPA – ₹14 LPA

Actual compensation depends on experience, skills, interview performance, and location.

How to Apply

Interested candidates can send their updated CV to:

Email: vaishnavinandkishor.kamble@iqvia.com With Current CTC And expected CTC and Notice period in Subject

Ensure your resume highlights:

• Clinical Data Management experience
• Medidata Rave expertise
• EDC knowledge
• Database Lock experience
• Query Management
• Clinical Trials exposure