Job Summary
Medpace, a globally recognized Contract Research Organization (CRO), is looking for a dedicated IRT Validator to join its Randomization and Study Product Management team in Navi Mumbai, India. This full-time, office-based role plays a pivotal part in clinical trial management and offers exciting career growth opportunities within the global pharmaceutical and healthcare industry.
Key Responsibilities
Develop and implement test plans for clinical trial systems.
Execute test plans and prepare comprehensive validation packages.
Review validation packages prepared by other team members.
Analyze and validate requirement specification documents from internal clients.
Validate both new projects and modifications to existing projects ensuring compliance with industry standards.
Required Skills & Qualifications
Bachelor's degree in Mathematics, Computer Science, or related field.
Proven ability to complete validation activities within strict timelines and quality standards.
Proficiency in English (spoken and written).
Familiarity with clinical data management and validation processes is preferred.
Perks & Benefits
Flexible work environment promoting work-life balance.
Competitive salary and benefits package.
Generous paid time off (PTO) plans.
Structured career development with clear growth pathways.
Company-sponsored employee events.
Access to health and wellness initiatives.
Company Description
Medpace is a leading global CRO offering Phase I-IV clinical development services to the pharmaceutical, biotech, and medical device sectors. With over 5000 professionals across 40+ countries, Medpace excels in therapeutic areas such as oncology, cardiology, CNS, and infectious diseases, supporting innovative and safe medical solutions worldwide.
Work Mode
On-site – Navi Mumbai, India
Call-to-Action
Looking to advance your career in clinical data management and validation? Apply now and become part of Medpace’s global mission to improve healthcare through clinical research excellence.
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