IQVIA Hiring Clinical DB Validation Specialist
- IQVIA Hiring Clinical DB Validation Specialist | Rave EDC | 2–4 Years | Multiple Locations (Hybrid)
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Skills Required:
- Experience:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What tools are required?
- What is the work mode?
- Are shifts mandatory?
- What is the career growth?
IQVIA Hiring Clinical DB Validation Specialist | Rave EDC | 2–4 Years | Multiple Locations (Hybrid)
IQVIA is hiring Clinical DB Validation Specialists across Kochi, Kolkata, Bangalore, Hyderabad, and Thane (hybrid model). This is a high-value opportunity for professionals with 2–4+ years of experience in clinical data management and database validation to work on global clinical trials using advanced EDC systems.
The company is offering multiple vacancies for this role, making it suitable for candidates with hands-on experience in Rave EDC, edit checks validation, and clinical database testing who want to grow in a leading global CRO.
Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial intelligence. The organization combines data science, technology, and domain expertise to accelerate drug development and improve patient outcomes worldwide.
With a strong global presence and involvement in large-scale clinical trials, IQVIA provides professionals with exposure to cutting-edge tools, global projects, and structured career progression in clinical data management and validation.
Job Role & Responsibilities
As a Clinical DB Validation Specialist, you will be responsible for validating clinical databases and ensuring data quality in electronic data capture systems.
Key responsibilities include:
- Perform independent testing of edit checks, database components, and SAS listings
- Validate clinical databases built in Rave EDC
- Design and review eCRFs (electronic Case Report Forms)
- Prepare and review specifications for database validation
- Ensure compliance with clinical data standards and regulatory requirements
- Identify data issues and ensure timely resolution
- Collaborate with cross-functional teams including data management and programming
This role is critical in ensuring data accuracy, integrity, and regulatory compliance in global clinical trials.
Eligibility / Qualifications
Candidates must meet the following educational requirements:
B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Biochemistry, Clinical Research
Skills Required:
- Strong experience in Clinical Database Validation
- Hands-on expertise with Rave EDC
- Knowledge of edit checks, SAS listings, and data validation processes
- Experience in eCRF design and specification writing
- Understanding of clinical trial processes and data standards
- Good communication and problem-solving skills
Experience:
- 2 to 4+ years of experience in clinical data management or validation roles
Location & Salary
- Locations: Kochi, Kolkata, Bangalore, Hyderabad, Thane
- Work Mode: Hybrid
- Shift: Flexible shifts (global project support)
- Salary: Competitive salary as per CRO and clinical data management industry standards
Application Process
Interested candidates can apply by sharing their updated resume:
Email: bharathi.n@iqvia.com
Early application is recommended due to high demand for Rave EDC and database validation roles.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, a minimum of 2 years of experience is required.
What tools are required?
Hands-on experience with Rave EDC and SAS listings is essential.
What is the work mode?
Hybrid across multiple locations in India.
Are shifts mandatory?
Yes, flexibility for global shift timings is required.
What is the career growth?
You can grow into roles like Senior Data Validation Specialist, Data Manager, or Clinical Data Lead.
| Category | Details |
|---|---|
| Company | IQVIA |
| Vacancies | Clinical DB Validation Specialist |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc/MSc Life Sciences, Biotechnology, Biochemistry |
| Experience | 2–4+ Years |
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