Global healthcare intelligence leader IQVIA is currently hiring experienced Clinical Data Specialists to strengthen its Clinical Data Management (CDM) team in India. This opportunity is ideal for professionals with 2.5–6 years of clinical data management experience, particularly those skilled in Rave EDC, clinical trial data review, and study lifecycle management.
The Clinical Data Specialist role at IQVIA offers exposure to global clinical trials, advanced data management technologies, and collaboration with international pharmaceutical and biotechnology clients.
If you are looking for Clinical Data Management jobs in Bangalore, Thane, Kochi, or Kolkata, this position provides an excellent opportunity to advance your career in clinical research.
Job Overview
- Job Role: Clinical Data Specialist
- Company: IQVIA
- Department: Clinical Data Management (CDM)
- Experience Required: 2.5 – 6 Years
- Employment Type: Full-Time
- Work Model: Hybrid / Office-based
- Locations: Bangalore, Thane, Kochi, Kolkata
Key Responsibilities
Professionals hired for the IQVIA Clinical Data Specialist role will be responsible for:
- Managing clinical trial data management activities across study lifecycle stages including startup, conduct, and closeout
- Working with Rave EDC systems for data entry validation and query management
- Reviewing clinical data to ensure accuracy, consistency, and regulatory compliance
- Coordinating with clinical operations, biostatistics, and regulatory teams
- Leading study-level data management activities and supporting global clinical trials
- Performing data cleaning, discrepancy management, and database lock activities
- Communicating with sponsors and stakeholders to ensure timely data delivery
- Supporting clinical study documentation and data quality standards
Required Qualifications
Candidates interested in Clinical Data Specialist jobs at IQVIA should meet the following requirements:
Education
- Bachelor’s or Master’s degree in:
- Life Sciences
- Pharmacy (B.Pharm / M.Pharm)
- Biotechnology
- Clinical Research
- Related biomedical sciences field
Experience
- 2.5 – 6 years of experience in Clinical Data Management
- Hands-on experience with Rave EDC
- Experience across study startup, conduct, and closeout
- Ability to manage study deliverables independently
Skills
- Strong understanding of Clinical Data Management processes
- Knowledge of GCP guidelines and clinical trial regulations
- Experience with clinical database review and discrepancy management
- Ability to interact with clients and global teams
- Comfortable working in shift-based hybrid or office environments
Why Join IQVIA?
IQVIA is one of the world’s largest clinical research and healthcare analytics organizations, supporting pharmaceutical innovation globally.
Key benefits of working with IQVIA include:
- Exposure to global clinical trials
- Opportunities to work with leading pharmaceutical sponsors
- Strong career growth in Clinical Data Management and CRO operations
- Advanced technology platforms like Rave EDC
- Collaborative international work environment
How to Apply
Interested candidates can apply by sending their updated CV to:
Applicants should include:
- Updated Resume
- Current Experience in Clinical Data Management
- Expertise in Rave EDC
- Current Location & Preferred Location
Early applications are recommended due to high demand for Clinical Data Management professionals in CRO companies like IQVIA.