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Medpace

Global CRO delivering full-service clinical trials

Software Engineer

Full-Stack EngineeringConfirmed live in the last 24 hours
Full-timeDenver, CO, USA

About the Job

Requirements

  • A Bachelor's degree in Computer Science is required.
  • Software development experience using C#, Angular or a similar JavaScript framework, HTML5, CSS3, SQL, and GitHub is required.
  • Experience with the software development life cycle (SDLC), including release management, is required.
  • Excellent analytical, written, and oral communication skills are required.
  • Excellent computer skills are required.

Responsibilities

  • Contribute to software development teams for one or multiple software applications or initiatives.
  • Build software applications and features in an Agile environment by following the software development life cycle (SDLC) process.
  • Develop applications in a hybrid and cloud-native setting using object-oriented programming (C#), databases (SQL), Entity Framework (EF), Angular, and web applications (ASP.NET).
  • Contribute to requirements gathering, design, development, testing, release, and maintenance support of applications.
  • Collaborate with team members regarding projects, development, tools, and training.
  • Perform high-level end-user support, including feature training and troubleshooting for applications.
  • Contribute to the software validation process through development, review, and/or execution of test plans, test cases, and scripts.
  • Provide technical assistance for junior team members.
  • Learn patterns, approaches, and business practices across multiple development teams.

Desired Qualifications

  • Prior experience using Azure and Entity Framework is a plus.
  • Prior experience modernizing systems is a plus.

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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