IQVIA, one of the world’s leading healthcare and clinical research organizations, is hiring Clinical Data Specialists (CDS/CDA) across multiple locations in India. This opportunity is ideal for professionals with 1-6 years of Clinical Data Management (CDM) experience and hands-on expertise in Medidata Rave, Veeva, database design, data review, study startup, conduct, and closeout activities.
Candidates with B.Pharm, B.Sc, or M.Sc backgrounds looking to build a long-term career in Clinical Data Management should not miss this opportunity.
Job Overview
- Company: IQVIA
- Position: Clinical Data Specialist (CDS/CDA)
- Experience: 1-6+ Years
- Job Type: Full-Time
- Work Mode: Hybrid
- Locations: Hyderabad, Bengaluru, Pune, Kochi, Kolkata, Thane
- Industry: Pharmaceutical & Life Sciences
- Department: Research & Development
Key Responsibilities
As a Clinical Data Specialist at IQVIA, you will:
- Support Clinical Data Management activities for global clinical trials.
- Perform clinical data review and data validation.
- Write, review and resolve Data Clarification Forms (DCFs).
- Develop, configure and test clinical databases.
- Create and review edit specifications.
- Perform User Acceptance Testing (UAT) and database testing.
- Support study startup, conduct and closeout activities.
- Lead database audit activities when required.
- Perform clinical data coding.
- Serve as a Data Operations Coordinator (DOC) for assigned studies.
- Maintain compliance with SOPs, ICH-GCP and internal quality standards.
- Collaborate with cross-functional global clinical teams.
Required Qualifications
Education
Candidates with any of the following qualifications are eligible:
- B.Pharm
- B.Sc
- M.Sc
- Bachelor’s degree in Clinical Sciences
- Biological Sciences
- Mathematical Sciences
- Equivalent education and relevant experience
Required Skills
Preferred candidates should possess experience in:
- Clinical Data Management (CDM)
- Medidata Rave
- Rave EDC
- Veeva
- Database Design
- Database Testing
- Data Review
- Data Validation
- Data Clarification Forms (DCF)
- Clinical Data Coding
- Study Startup
- Study Conduct
- Study Closeout
- Clinical Database Audit
- Medical Terminology
- Excellent Communication Skills
- Attention to Detail
Why Join IQVIA?
IQVIA offers professionals the opportunity to work on global clinical research projects while gaining exposure to advanced Clinical Data Management technologies.
Benefits include:
- Hybrid work model
- Global clinical trial exposure
- Career growth opportunities
- Exposure to Medidata Rave and Veeva platforms
- International project experience
- Learning and development programs
- Collaborative work environment
Preferred Candidate Profile
Ideal candidates should have:
- 1-6 years of Clinical Data Management experience
- Hands-on experience with Medidata Rave
- Knowledge of Veeva applications
- Experience in clinical database testing
- Understanding of study startup and closeout
- Strong analytical and organizational skills
- Good understanding of medical terminology
How to Apply
