IQVIA Hiring Associate Clinical Data Coordinator | Multiple India Locations | Hybrid
Are you seeking IQVIA Careers India or Clinical Data Management Jobs? Leading global Contract Research Organization (CRO) IQVIA is hiring an Associate Clinical Data Coordinator across multiple locations in India.
This hybrid CDM opportunity is ideal for pharmacy and life science professionals with 1 to 2 years of experience in database setups, EDC systems, and clinical trial coordination. To draft a resume detailing your EDC and Medidata Rave experience, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | IQVIA |
| Position | Associate Clinical Data Coordinator |
| Job Locations | Kochi, Kolkata, Thane, Hyderabad, Bengaluru, Pune |
| Department | Clinical Data Management (CDM) |
| Employment Type | Full-Time |
| Work Model | Hybrid |
| Experience Required | 1 – 2 Years in CDM |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc in Life Sciences, Biotechnology or related fields |
| Expected Salary | ₹4.8 LPA – ₹7.2 LPA (Estimated) |
💼 Key Responsibilities
- Study Life Cycle Support: Assist study teams with Clinical Data Management tasks across Study Set-Up, Study Conduct, and Database Lock/Closeout.
- Database Coordination: Build and update EDC systems (specifically Medidata Rave) to ensure high-quality database standards.
- Data Cleaning: Run edit check scripts, analyze clinical data inconsistencies, and log database queries.
- Query Management: Reconcile clinical queries with investigator sites to ensure protocol data validation and consistency.
- SOP Compliance: Ensure clinical data tracking complies with GCP regulations, company SOPs, and regulatory requirements.
- Cross-Functional Cooperation: Work with global medical writers, clinical trial assistants, and safety leads to ensure data integrity.
To learn how clinical data coordinator salaries compare to drug safety and pharmacovigilance specialist structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology, or a related discipline.
- Experience: 1 to 2 years of relevant experience in Clinical Data Management (CDM).
- EDC Systems: Hands-on experience working with Electronic Data Capture platforms, specifically Medidata Rave.
- Methodology Knowledge: Basic understanding of GCP rules, study set-up documents, edit check specifications, and database validation workflows.
- Communication: Good written and verbal English communication skills for collaborating with global study managers.
- Flexibility: Comfortable working in shift-based operations depending on global project demands.
For pharmacy graduates analyzing clinical data operations compared to conventional formulation laboratory careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join IQVIA?
- Opportunity to work with the world's largest clinical research and analytics provider.
- Gain advanced training in industry-leading CDM platforms, including Medidata Rave.
- Hybrid working environment providing optimal work-life balance.
- Mentorship under global industry experts with clear career progression paths.
To test your basic knowledge of clinical trials, protocol definitions, and GCP terms before your technical interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Clinical Data Coordinator vs Healthcare IT
Clinical Data Coordinators manage database entry specifications, data validation edit checks, and database locks to support global clinical trials, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for IQVIA CDM Candidates
- Specify Rave Experience: Clearly mention the duration and specific functions (e.g. query generation, form design, data cleaning) you performed in Medidata Rave.
- Detail Study Phases: List the phases of clinical trials (e.g., Phase I-IV) and therapeutic areas (e.g., oncology, cardiovascular) you have supported.
- Highlight Database Milestones: Explicitly mention if you have participated in database design, User Acceptance Testing (UAT), or actual Database Lock events.
💬 IQVIA Associate Clinical Data Coordinator Interview Questions
- Q1. What is the difference between Study Conduct and Study Closeout in CDM?
Answer Guidance: Study Conduct involves ongoing data cleaning, generating queries, reconciling external data, and performing database reviews. Study Closeout involves finalizing data reviews, resolving all pending queries, locking the database, and archiving trial documentation. - Q2. What is an Edit Check in clinical data coordination?
Answer Guidance: An Edit Check is an automated logic script programmed within the EDC system to identify discrepancies or errors in the entered clinical data (e.g., checking if a patient's visit date is prior to their screening date). - Q3. How do you handle a scenario where an investigator site does not respond to database queries?
Answer Guidance: I would follow up systematically according to communication protocols, track the query status in our logs, escalate to the Clinical Research Associate (CRA) or monitor responsible for the site, and keep the study manager informed.
🚀 How to Apply?
Interested and eligible candidates can share their updated CV directly with IQVIA's recruitment coordinator via email:
📧 Apply Via Email: vaishnavinandkishor.kamble@iqvia.com(Use Subject line: Application for Associate Clinical Data Coordinator)
❓ Frequently Asked Questions
Q. What is the required experience for this IQVIA data coordinator role?
Candidates should possess 1 to 2 years of relevant experience in Clinical Data Management (CDM).
Q. Is this position hybrid or full-time office?
This is a full-time position utilizing a hybrid work model across IQVIA's offices in India.
Q. How can I apply for this Associate CDC opening?
You can apply by sending your updated resume directly to the recruitment coordinator email: vaishnavinandkishor.kamble@iqvia.com.
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