Overview
Job Description
Medpace is expanding its clinical operations and is seeking a full-time, office-based IRT Validator to join the Randomization and Study Product Management team in Mumbai, India. The role supports the clinical trial management process and contributes to validation activities within the Biometrics department.
This position allows individuals to apply their existing knowledge while building further expertise within clinical research and data management operations.
Responsibilities
- Create and prepare detailed test plans.
- Execute test plans and assemble validation packages.
- Review validation documentation prepared by other team members.
- Assess requirement specification documents submitted by internal stakeholders.
- Validate new projects and manage validation updates for existing studies.
About Medpace
Medpace is a full-service clinical contract research organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. The organization focuses on advancing the global development of safe and effective medical therapies through a disciplined scientific approach.
The company utilizes regulatory and therapeutic expertise across key areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, antiviral, and anti-infective research. Medpace is headquartered in Cincinnati, Ohio and employs more than 5,000 professionals across 40+ countries.
Why Medpace
Medpace emphasizes people, purpose, and passion. The organization aims to contribute to improving the lives of patients and families affected by a wide range of diseases worldwide.
Employee Benefits
- Flexible work environment
- Competitive compensation and benefits
- Generous PTO offerings
- Structured career development paths with growth opportunities
- Company-sponsored employee appreciation events
- Health and wellness initiatives
Awards
- Recognized by Forbes among America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
- Recipient of multiple CRO Leadership Awards from Life Science Leader magazine for expertise, quality, reliability, and capabilities
What to Expect Next
Applications are reviewed by the Medpace team. Qualified candidates will be contacted with details regarding the next steps in the recruitment process.
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Key Skills
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Education Requirements
- Bachelor’s degree in Mathematics, Computer Science, or a related field
Eligible Batch Years
Medpace
Medpace is a global, full-service clinical contract research organization (CRO) headquartered in Cincinnati, Ohio, USA. Founded in 1992, the company specializes in providing comprehensive development services to the biotechnology, pharmaceutical, and medical device industries. Medpace's mission is to accelerate the development of safe and effective medical treatments through scientifically-driven, high-quality clinical research. With a focus on therapeutic areas such as oncology, cardiology, metabolic disease, and infectious disease, Medpace offers expertise across all phases of clinical trials.
Employing over 5,000 professionals worldwide, Medpace has built a strong reputation for its integrated approach, combining regulatory, medical, and operational expertise to deliver efficient and reliable results. The company operates in multiple countries, enabling it to manage global trials with localized knowledge. In recent years, Medpace has reported steady growth and strong financial performance, reflecting increasing demand for outsourced clinical research services. Its commitment to quality and scientific rigor has positioned it as a trusted partner for sponsors seeking to bring innovative therapies to market.
Company Details
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Websitemedpace.com