Clinical Data Manager

☞ Medpace

전망: 140

갱신일: 26-11-2025

위치: Leuven Flemish Brabant

범주: R & D IT-소프트웨어

산업: Biotechnology Research

수평: Mid-Senior level

직업 종류: Full-time

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작업 내용

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Manager to join our Data Management team in Leuven. 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 and review data management procedures for clinical trials with sponsor companies and other departments;
  • Design reports and metrics that are useful management tools for your projects
  • Lead the design and validation of the CRF specifications and edit checks for the electronic data capt system used for each study
  • Attend and participate in teleconferences and face-to-face meetings with sponsor companies as the representative from data management
  • Manage multiple projects and associated project team members: and
  • Coordinate overall data management by serving as primary contact for the sponsor, external data providers, and all project team members;
Requirements

Qualifications
  • Minimum Bachelor’s degree and at least four (4) years of Data Management experience or Master degree and at least two (2) years of Data Management experience
  • Computer experience with database, spreadsheet, and analysis software (i.e. SAS,InForm and Rave preferred);
  • Possess an understanding of database structure and processes in data managment; and
  • A basic knowledge of medical terminology is needed, as well as knowledge of clinical research methodologies.
We kindly ask to send applications in English.

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?

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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마감 시간: 10-01-2026

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