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Medpace

Global CRO delivering full-service clinical trials

R Programmer

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeDenver, CO, USA

About the Job

Requirements

  • A bachelor's degree in informatics, computer science or engineering, biomedical engineering, health information, statistics, or a related field is required.
  • A minimum GPA of 3.6 is required.
  • Programming experience in R is required.
  • Work experience with clinical data is required.
  • The ability to prioritize multiple projects on a sprint schedule is required.
  • Analytical thinking and attention to detail are required.
  • Verbal communication skills are required.

Responsibilities

  • Evaluate data needs for assigned projects and recommend a strategic approach specific to the study design.
  • Work alongside operational and medical leads to contribute data products, primarily Shiny applications.
  • Contribute to internal R package development to support efficient cross-departmental programming practices.
  • Interact with relational data at study and enterprise levels, including querying, wrangling, analyzing, and reporting.
  • Develop algorithms to describe, classify, and predict operational outcomes of clinical trials.
  • Support departmental process-improvement initiatives.
  • Collaborate with Clinical Operations teams to identify needs and establish solutions involving data analytics, visualization, and accessibility.
  • Evaluate study protocols and collaborate with Clinical Trial Managers to develop and validate data products that increase operational efficiency.
  • Support custom and enterprise-wide solutions in collaboration with software engineering teams.

Desired Qualifications

  • Experience building web applications using Shiny or Streamlit is preferred.
  • Experience building dashboards using Power BI, Tableau, or Spotfire is 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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