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FULL TIME

Clinical Database Programmer

Medpace
Mumbai
₹10 - ₹18 LPA
Posted 1/22/2026
About the Role

Roles & Responsibilities
• Develop, program, validate, and maintain clinical trial databases in compliance with company SOPs and regulatory standards
• Design and maintain CDASH-compliant Case Report Forms (CRFs) and support the standard CRF library
• Perform Medidata RAVE study build activities including database setup, edit checks, and custom functions
• Develop and implement custom functions using C# programming within Medidata RAVE
• Act as the primary technical point of contact for Data Management teams on assigned clinical studies
• Ensure high-quality database design, validation documentation, and audit readiness
• Provide technical support throughout the clinical trial lifecycle from study startup to database lock
• Support global clinical trials across multiple therapeutic areas


Qualification

• Bachelor’s or Advanced degree in Life Sciences, Computer Science, or equivalent


Experience

• Minimum 3+ years of experience in Clinical Database Programming
• Hands-on experience in Medidata RAVE study build and maintenance
• Experience working in CRO, pharma, or biotech clinical research environments


Skills

• Strong expertise in Medidata RAVE (study build, edit checks, custom functions)
• Proficiency in Custom Functions and C# programming
• Knowledge of CDASH standards and CRF design principles
• Familiarity with Veeva EDC is an added advantage
• Understanding of clinical data management and regulatory requirements
• Excellent documentation and validation skills
• Strong attention to detail and quality mindset
• Effective communication and cross-functional collaboration skills


About the Organisation

Medpace is a globally recognized Clinical Research Organization (CRO) with more than three decades of experience supporting Phase I–IV clinical trials across multiple therapeutic areas. Known for its scientific-driven approach and strong in-house expertise, Medpace offers a stable, growth-oriented environment where clinical research professionals can build long-term careers while contributing to global drug development programs.

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