IQVIA is inviting applications for the position of Associate Clinical Data Coordinator across multiple locations in India. This opportunity is ideal for professionals with 2+ years of Core Clinical Data Management (CDM) experience who have worked throughout the complete clinical study lifecycle. Candidates with expertise in Medidata Rave EDC, Veeva EDC, CRF design, UAT, edit checks, query management, data cleaning, external data reconciliation, and database lock activities are encouraged to apply.
If you’re looking for an exciting Clinical Data Management job at IQVIA, this role offers excellent career growth, exposure to global clinical trials, and the opportunity to work in a collaborative hybrid environment.
Job Overview
| Particular | Details |
|---|---|
| Company | IQVIA |
| Position | Associate Clinical Data Coordinator |
| Department | Clinical Data Management |
| Experience | Minimum 2 Years |
| Job Type | Full-Time |
| Work Mode | Hybrid / Office-Based |
| Locations | Thane, Bangalore, Kochi, Kolkata |
Key Responsibilities
As an Associate Clinical Data Coordinator, you will:
- Support end-to-end Clinical Data Management activities.
- Participate in study start-up, study conduct, and study close-out.
- Design and review Case Report Forms (CRFs).
- Perform User Acceptance Testing (UAT) for EDC systems.
- Validate edit checks and perform data cleaning activities.
- Manage clinical data queries and resolve discrepancies.
- Reconcile external clinical data sources.
- Track study metrics and generate progress reports.
- Support database lock and study close-out processes.
- Ensure compliance with ICH-GCP, SOPs, and sponsor requirements.
Required Qualifications
Candidates should possess:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Clinical Research, Nursing, or related healthcare discipline.
- Minimum 2 years of hands-on Core Clinical Data Management experience.
- Experience across:
- Study Start-up
- Study Conduct
- Study Close-out
- Strong experience with:
- Medidata Rave EDC and/or Veeva EDC
- CRF Design & Review
- UAT
- Edit Check Validation
- Data Cleaning
- Query Management
- External Data Reconciliation
- Study Metrics Reporting
- Database Lock Activities
Not Eligible
The following profiles are not eligible if their experience is primarily in:
- Clinical Research Associate (CRA)
- Clinical Research Coordinator (CRC)
- Pharmacovigilance
- Trial Master File (TMF)
- Quality Assurance (QA) / Quality Functions
Preferred Skills
- Strong Clinical Data Management knowledge
- Excellent analytical and problem-solving abilities
- Experience with Medidata Rave or Veeva EDC
- Good understanding of ICH-GCP guidelines
- Attention to detail
- Effective communication skills
- Team collaboration and stakeholder management
Why Join IQVIA?
Working with IQVIA provides:
- Opportunity to work on global clinical trials
- Exposure to industry-leading EDC platforms
- Hybrid working environment
- Career progression in Clinical Data Management
- Learning from experienced global teams
- Competitive compensation and employee benefits
- International quality standards and best practices
How to Apply
If your experience matches the eligibility criteria:
- Update your latest CV.
- Highlight your Clinical Data Management experience, including Rave/Veeva expertise.