IQVIA Hiring Clinical Data Management (Associate Clinical Data Coordinator)
- IQVIA Clinical Data Management Jobs: Associate Clinical Data Coordinator (Hybrid Roles)
- Why Choose a Career at IQVIA?
- Industry-Leading Clinical Research Organization
- Hybrid Work Culture
- Key Responsibilities
- What Will You Be Doing?
- Qualification & Skill Requirements
- Who Can Apply?
- Location & Mode of Work
- High-CPC Keywords Targeted:
- Call to Action
- Summary Table
Clinical Data Coordinator Jobs for BSc/MSc/BPharm Graduates – 1+ Yr Experience at IQVIA (Hybrid, Multiple Cities)
Apply for Associate Clinical Data Coordinator positions at IQVIA in Thane, Bangalore, and Hyderabad. 1–2 years of experience required; hybrid work model
IQVIA Clinical Data Management Jobs: Associate Clinical Data Coordinator (Hybrid Roles)
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📱 Join Click HereIf you have a background in clinical data management and are looking for a role in a global pharmaceutical services company, IQVIA offers an excellent opportunity to grow your career. IQVIA is currently hiring Associate Clinical Data Coordinators at its Thane, Bangalore, and Hyderabad locations.
These hybrid work model roles are ideal for candidates with 1–2 years of relevant experience in Clinical Data Management (CDM), particularly those familiar with data entry, validation, and clinical trial data review processes. If you’re passionate about delivering clinical trial results efficiently and accurately, this role is designed for you.
Why Choose a Career at IQVIA?
Industry-Leading Clinical Research Organization
IQVIA is a globally recognized Contract Research Organization (CRO) that integrates data science, technology, and human expertise to advance healthcare outcomes. As a Clinical Data Coordinator, you’ll be working on real-world data that drives regulatory decisions and patient safety.
Hybrid Work Culture
IQVIA supports a flexible working model, combining in-office collaboration with remote work options to foster productivity and work-life balance.
Key Responsibilities
What Will You Be Doing?
- Coordinate clinical trial data entry and cleaning activities across multiple study sites
- Maintain and validate data using Clinical Data Management Systems (CDMS)
- Track discrepancies and query resolutions in compliance with ICH-GCP standards
- Collaborate with clinical research associates, biostatisticians, and project managers
- Support documentation, metrics tracking, and audit readiness
Qualification & Skill Requirements
Who Can Apply?
- Education: BSc, MSc (Life Sciences), or B.Pharm degree holders
- Experience: 1 to 2 years of experience in CDM or related clinical research domain
- Skills: Strong communication, familiarity with MedDRA coding, CDMS tools (e.g., Rave, Oracle Clinical), data query resolution
Location & Mode of Work
IQVIA is currently hiring for the following locations:
- Thane (Maharashtra)
- Bangalore (Karnataka)
- Hyderabad (Telangana)
Work Mode: Hybrid (office-based + remote)
High-CPC Keywords Targeted:
- Clinical Data Management Jobs
- Associate Clinical Data Coordinator
- Clinical Research Jobs for BSc/MSc/BPharm
- Hybrid Pharma Jobs in India
- CRO Jobs in Bangalore Hyderabad
Call to Action
If you meet the criteria and are ready to elevate your career in clinical data coordination, apply today. Ensure your resume is up to date and highlights your experience in CDM tools and processes.
To Apply: Share your resume via IQVIA’s official career portal or reach out to their recruitment email if specified in the original listing.
Summary Table
| Company Name | IQVIA |
|---|---|
| Current Vacancies in Departments | Clinical Data Management (Associate Clinical Data Coordinator) |
| Required Education | BSc, MSc (Life Sciences), B.Pharm |
| Experience Required | 1 to 2 years |
| Location | Thane, Bangalore, Hyderabad (Hybrid) |
To apply for this job please visit IQVIA's%20official%20career%20portal.