IRT Validator

Roles & Responsibilities
• Develop detailed validation test plans for IRT (Interactive Response Technology) systems
• Execute validation test plans and prepare validation documentation packages
• Review requirement specification documents from internal stakeholders
• Review and verify validation documents prepared by team members
• Validate new IRT projects and updates to existing randomization and drug supply systems
• Ensure validation activities are completed within defined timelines and quality standards
• Support clinical trial randomization, investigational product management, and regulatory compliance

Qualification
• Bachelor’s degree in Mathematics, Computer Science, or related field

Experience
• Experience in clinical trial data management, system validation, or software testing preferred
• Exposure to IRT / IVRS / IWRS systems is an added advantage

Skills
• Strong analytical and problem-solving abilities
• Knowledge of system validation and documentation standards
• High attention to detail and quality compliance
• Ability to manage tasks within strict timelines
• Good written and spoken English communication
• Team collaboration and cross-functional coordination skills

About the Organization
Medpace is a global Clinical Research Organization (CRO) headquartered in Cincinnati, Ohio, operating in over 40 countries with 5,000+ employees. The company provides comprehensive clinical development services across multiple therapeutic areas and is recognized by Forbes and CRO Leadership Awards for its excellence in clinical research.