Experienced Clinical Database Programmer (Hybrid)

☞ Medpace

見る: 135

更新日: 16-11-2025

場所: Leuven Flemish Brabant

カテゴリー: IT-ソフトウェア

業界: Biotechnology Research

レベル: Associate

ジョブタイプ: Full-time

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仕事内容

Job Summary

Our global activities are growing rapidly, and we are currently seeking a full-time, office/home-basedExperienced Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Develop, program, validate and maintain clinical trial electronic data capture (EDC) databases according to company standards;
  • Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards;
  • Perform integration testing to QC the database;
  • Support a team via managing system changes to the database throughout the course of a project;
  • Maintain study documentation.
Qualifications
  • Bachelor’s degree (BSc), preferably in life sciences or a technical field;
  • Atleast 1 year of Medidata Rave programming experience, including post go-live migrations’
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office;
  • An interest in programming languages is preferred;
  • Knowledge of medical terminology is preferred;
  • Excellent verbal and written communication skills;
  • Ability to work in a team environment with data managers, data coordinators, statisticians, and programmers; and
  • Meticulous attention to detail.
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 4,000 people across almost 40 countries.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Awards
  • Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
  • Recognized by Forbes as one of America’s Best Mid-size Companies in 2021
  • Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
  • Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati
What To Expect Next

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets
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締切: 31-12-2025

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