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Medpace
Lyon, France (on-site)
12 hours ago
Genentech
Hillsboro, Oregon, United States (on-site)
10 days ago
Genentech
Hillsboro, Oregon, United States (on-site)
29 days ago
Medpace
Lyon, France
(on-site)
12 hours ago
Job Type
Full-Time
Job Function
Industry Research

Description

Our imaging services are rapidly growing, and we are currently seeking a full-time Software Engineer to join our team validating the new developments of our web application and backend quantification applications for the management and analysis of medical images and more (CT, MRI, PET, US, ECG, etc.).

Responsibilities

Responsibilities
  • Collect functional requirements and define acceptance criteria for the new developments of our web application.
  • Identifying complex validation strategies and scenarios to test functionalities of the web application to cover all functional requirements and acceptance criteria.
  • Write validation scripts in a highly regulated environment (clinical trial) and execute them for documentation.
  • Follow the company's software development lifecycle processes, working with developers.
  • Communicate with team members regarding projects, development, tools, and procedures.
  • Provide end-user support including setup, installation, and maintenance for applications released, as well as supporting users in resolution of bugs.
  • Write technical and user documentation.


Qualifications

  • Bachelor's Degree in Computer Science or equivalent, or higher
  • Experience in software development or validation
  • Well organized and meticulous
  • Other appreciated skills/knowledge:
    • Full-stack software development skills: C#, Typescript/Javascript, Angular
    • Code management tools: Azure DevOps, Git, etc.
    • Software Lifecycle Management applications
  • Team spirit
  • Good level of written and spoken English

The role is open to recruit at all levels

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks
  • Hybrid work-from-home options (dependent upon position and level)
  • Competitive PTO packages
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Flexible work schedule
  • Competitive compensation and benefits package
  • Structured career paths with opportunities for professional growth

Awards
  • Recognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022 and 2023
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility


What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets

Job ID: 73965051
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