IQVIA is hiring Clinical Data Coordinators for its offices in Kochi and Bangalore. This is an excellent opportunity for experienced Clinical Data Management (CDM) professionals who have worked on global clinical trials and possess hands-on experience with Medidata Rave (Rave EDC), Query Management, User Acceptance Testing (UAT), and Vendor Reconciliation.
If you have 1.5โ2.5 years of Clinical Data Management experience and are looking to advance your career with one of the world’s leading clinical research organizations, this opportunity is worth considering.
Job Details
| Particular | Details |
|---|---|
| Company | IQVIA |
| Job Title | Clinical Data Coordinator |
| Job Type | Full-Time |
| Work Mode | Office-Based |
| Working Days | 5 Days a Week |
| Experience | 1.5โ2.5 Years |
| Locations | Kochi, Kerala & Bangalore, Karnataka |
| Industry | Clinical Research / Clinical Data Management |
Key Responsibilities
As a Clinical Data Coordinator at IQVIA, you will:
- Support clinical data management activities throughout the study lifecycle.
- Perform study start-up, conduct, and close-out activities.
- Manage clinical data queries and ensure timely resolution.
- Work extensively with Medidata Rave (Rave EDC).
- Participate in User Acceptance Testing (UAT).
- Perform Vendor Reconciliation activities.
- Review Manual Listings for data consistency and quality.
- Ensure compliance with GCP, SOPs, and sponsor requirements.
- Collaborate with cross-functional global clinical teams.
- Maintain high standards of clinical data quality and integrity.
Required Qualifications
Candidates should possess:
- Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, Microbiology, Biochemistry, Nursing, or related Life Science discipline
- 1.5โ2.5 years of Clinical Data Management experience
- Mandatory experience with Medidata Rave / Rave EDC
- Strong knowledge of:
- Clinical Data Management
- Query Management
- User Acceptance Testing (UAT)
- Vendor Reconciliation
- Manual Listings Review
- Excellent written and verbal communication skills.
Preferred Skills
Ideal candidates will have:
- Experience working on global clinical trials.
- Strong understanding of clinical data quality processes.
- Knowledge of regulatory compliance and GCP.
- Ability to work with cross-functional international teams.
- Strong analytical and problem-solving skills.
Why Join IQVIA?
Working at IQVIA offers several advantages:
- Opportunity to work with one of the world’s leading CROs.
- Exposure to global clinical trials.
- Career growth in Clinical Data Management.
- Collaborative international work environment.
- Learning opportunities on advanced clinical technologies.
- Stable long-term career path in clinical research.
Salary (Estimated)
Based on current market trends for Clinical Data Coordinators in India:
Estimated Salary: โน5.5 LPA โ โน8.5 LPA
Actual compensation may vary depending on experience, skills, interview performance, and company policies.
How to Apply
Interested candidates can send their updated resume to:
Email: angeline.preethy@iqvia.com
Before applying:
Highlight projects involving global clinical trials.
Update your resume with Medidata Rave experience.
Mention UAT, Query Management, Vendor Reconciliation, and Study Lifecycle experience.