IQVIA is actively hiring Clinical Data Specialists for its Clinical Data Management (CDM) team across multiple locations in India. This opportunity is ideal for professionals with 2-5 years of Clinical Data Management experience who are looking to advance their careers in clinical research, clinical data review, and electronic data capture (EDC) systems.
Candidates with hands-on experience in clinical trial data management, query management, data clarification, and Medidata Rave are encouraged to apply. The position offers exposure to global clinical studies, leadership development opportunities, and a collaborative hybrid work environment.
Job Details
| Particulars | Details |
|---|---|
| Position | Clinical Data Specialist |
| Company | IQVIA |
| Job Type | Full-Time |
| Work Mode | Hybrid |
| Experience | 2-5 Years |
| Industry | Clinical Research / Clinical Data Management |
| Locations | Kolkata, Pune, Thane, Kochi, Bangalore, Hyderabad |
| Qualification | Bachelor’s Degree in Clinical, Biological, Mathematical Sciences or related field |
Key Responsibilities
As a Clinical Data Specialist at IQVIA, you will:
- Support end-to-end Clinical Data Management activities.
- Review and validate clinical trial data for accuracy and completeness.
- Perform data review and query management activities.
- Resolve data discrepancies through data clarification processes.
- Work with Electronic Data Capture (EDC) systems such as Medidata Rave.
- Collaborate with Data Operations Coordinators (DOCs), Data Team Leads (DTLs), and Functional Managers.
- Ensure compliance with clinical research regulations and company standards.
- Support high-quality data delivery for global clinical studies.
- Participate in leadership and mentoring responsibilities within the CDM team.
Required Skills
Applicants should possess:
- 2-5 years of experience in Clinical Data Management (CDM).
- Strong understanding of the clinical trial lifecycle and clinical research processes.
- Experience in data review and query resolution.
- Hands-on experience with Medidata Rave or similar EDC platforms.
- Knowledge of medical terminology.
- Excellent organizational and communication skills.
- Strong attention to detail and quality-focused mindset.
Important Note
This opportunity is specifically for professionals with Clinical Data Management experience. Profiles from Pharmacovigilance (PV), Quality Control (QC), Clinical Research Coordinator (CRC), or Programming backgrounds may not be suitable unless they possess relevant CDM experience.
Educational Qualifications
Candidates should hold a Bachelor’s degree in:
- Clinical Sciences
- Biological Sciences
- Mathematical Sciences
- Life Sciences
- Related Healthcare Disciplines
Equivalent relevant experience may also be considered.
Why Join IQVIA?
IQVIA offers professionals an opportunity to work on cutting-edge clinical research projects while developing their expertise in clinical data management.
Benefits Include:
- Exposure to global clinical trials
- Hybrid work model
- Career growth and leadership opportunities
- Collaborative and learning-focused environment
- Work with advanced clinical data management technologies
- Professional development within a globally recognized CRO
Job Locations
Selected candidates may be placed at any of the following IQVIA offices:
- Pune
- Bangalore
- Hyderabad
- Kolkata
- Kochi
- Thane
How to Apply
Interested and eligible candidates can share their updated resume directly with the recruiter:
Email: angeline.preethy@iqvia.com