Looking for an Associate Clinical Data Coordinator job at IQVIA? Here’s an excellent opportunity for professionals with 1–2 years of Clinical Data Management (CDM) experience to join one of the world’s leading healthcare and clinical research organizations.

IQVIA is hiring Associate Clinical Data Coordinators for multiple locations across India. This hybrid Clinical Data Management job offers the opportunity to work on global clinical trials, collaborate with experienced teams, and build expertise in Medidata Rave, study setup, database lock, and clinical trial data management.

If you are looking for Clinical Data Management jobs in India, IQVIA jobs for CDM professionals, or Medidata Rave jobs, this opportunity is worth considering.

Job Overview

About IQVIA

IQVIA is a global leader in healthcare analytics, technology solutions, and clinical research services. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient outcomes worldwide.

Working at IQVIA provides professionals with exposure to international clinical studies, advanced clinical technologies, and career growth opportunities within the clinical research industry.

Associate Clinical Data Coordinator Responsibilities

As an Associate Clinical Data Coordinator, you will support clinical trial data management activities while ensuring high-quality and compliant clinical databases.

Key responsibilities include:

• Support clinical data management activities throughout the study lifecycle.
• Maintain quality, consistency, and integrity of clinical trial data.
• Participate in Study Set-Up activities.
• Assist during Study Conduct and ongoing database maintenance.
• Support Database Lock and Closeout activities.
• Work with study teams to resolve clinical data queries.
• Ensure compliance with SOPs, GCP, and regulatory requirements.
• Collaborate with cross-functional global teams.
• Maintain accurate clinical databases using Medidata Rave.

Required Qualifications

Applicants should possess:

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline.
• 1–2 years of Clinical Data Management experience.
• Working knowledge of Medidata Rave (EDC).
• Experience with:
  • Study Set-Up
  • Study Conduct
  • Database Lock
  • Study Closeout
• Strong analytical and communication skills.
• Ability to work in a collaborative environment.
• Flexibility to work in shift-based operations.

Preferred Skills

Candidates with the following skills will have an advantage:

• Clinical Data Management
• Electronic Data Capture (EDC)
• Medidata Rave
• Clinical Trial Documentation
• Database Validation
• Data Cleaning
• Query Management
• Good Clinical Practice (GCP)
• Attention to Detail
• Team Collaboration

Why Join IQVIA?

Joining IQVIA offers numerous career advantages:

• Work on global clinical research projects.
• Hybrid working model.
• Exposure to international clinical trials.
• Career advancement in Clinical Data Management.
• Learn from experienced industry professionals.
• Opportunity to work with advanced clinical technologies.
• Collaborative and innovation-driven work culture.

Work Locations

The position is available in the following cities:

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

Salary Expectations

Based on current Clinical Data Management market trends in India, the expected salary for this role is approximately:

₹4.8 LPA – ₹7.2 LPA (Estimated)

Actual compensation may vary depending on experience, skills, and company policies.

How to Apply

Interested candidates can share their updated resume directly via email:

Email: vaishnavinandkishor.kamble@iqvia.com

Applicants are encouraged to highlight their experience with Clinical Data Management, Medidata Rave, Study Setup, Database Lock, and Clinical Trial Operations in their CV.