Clinical Database Validation Specialist
Location: Kochi, India
Work Model: Hybrid
Employment Type: Full-Time
Job ID: R1521146
Company: IQVIA
About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences and healthcare industries. By leveraging advanced analytics, technology solutions, and deep domain expertise, IQVIA accelerates the development and commercialization of innovative medical treatments to improve patient outcomes worldwide.
Role Overview
IQVIA is seeking a Clinical Database Validation Specialist to support validation and testing activities within Clinical Data Management Systems (CDMS). This role is responsible for ensuring the accuracy, integrity, and regulatory compliance of clinical trial databases through comprehensive testing and validation practices. The position plays a critical role in delivering high-quality, inspection-ready databases that meet both internal standards and client requirements.
Key Responsibilities
Independently perform database validation and testing activities within CDMS environments
Validate edit checks, system configurations, SAS listings, transfer programming, and custom reports
Work across leading CDMS platforms including Oracle InForm, Medidata Rave, and OCRDC
Demonstrate strong understanding of clinical database structures and data flow
Ensure strict adherence to validation processes, SOPs, work instructions, and best practice guidelines
Maintain and update all validation-related documentation accurately and in a timely manner
Communicate project status, risks, and timelines to the Validation Team Lead or Manager
Escalate issues proactively to ensure timely resolution and project continuity
Mentor and guide Associate Validation Analysts in testing and validation activities
Conduct quality reviews of validation deliverables as required
Actively contribute to process improvement initiatives and continuous quality enhancement
Build and maintain effective working relationships with cross-functional and global teams
Required Qualifications and Experience
Bachelor’s degree in Science, Computer Science, Information Technology, or Bachelor of Technology (B.Tech)
1–2 years of hands-on experience in clinical database testing and validation using CDMS platforms
Minimum 2+ years of total professional experience in clinical data management or related roles
Practical experience with InForm, Medidata Rave, OCRDC, or similar CDMS tools
Strong understanding of clinical trial data standards, validation documentation, and regulatory expectations
Excellent analytical, documentation, and communication skills
Ability to work independently while collaborating effectively within cross-functional teams
Why Join IQVIA
Opportunity to work on global clinical trials with leading pharmaceutical and biotech sponsors
Exposure to industry-leading clinical data platforms and validation methodologies
Hybrid work model supporting flexibility and work-life balance
Structured career development, learning, and mentorship opportunities
Inclusive, collaborative, and innovation-driven work culture
Equal Opportunity Statement
IQVIA is committed to creating a diverse and inclusive workplace. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status. Reasonable accommodations are available throughout the recruitment process.
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