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Medpace

Global CRO delivering full-service clinical trials

Clinical Database Programmer

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNavi Mumbai, Maharashtra, IndiaNo salary listed

About the Job

Requirements

  • A Bachelor's or advanced degree in Life Sciences or Computer Science, or equivalent.
  • Excellent verbal and written communication skills.
  • Meticulous attention to detail.

Responsibilities

  • Develop, program, validate, and maintain clinical trial databases according to company standards.
  • Maintain and contribute to the company library of standard CDASH-compliant CRFs.
  • Act as the primary contact to the data management team for assigned studies, supplying necessary technical support and ensuring programming quality and adherence to company standards.

Desired Qualifications

  • Rave study-build and/or Veeva EDC experience in a similar position in the Pharma/Healthcare sector is preferred.
  • Custom function (C# programming) experience is preferred.
  • Certified Medidata Rave Study Builders are preferred.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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