Imaging Project Coordinator

il y a 3 semaines


Leuven, Flandre, Belgique Medpace Temps plein
Job Summary

Our imaging services are growing rapidly, and we are currently seeking a full-time Imaging Project Coordinator to join our team in Leuven. 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
  • Review incoming medical imaging data for clinical trials for initial quality standards.
  • Draft and maintain study-related documents (in English).
  • Contact with sites (hospitals) all around the world for qualification, follow-up, and queries.
  • Quality control of the received imaging data and transmittal forms.
  • Work on several projects with different teams.
  • Support the Project Manager with tasks such as data export requests and quality control.
  • Overall meeting support: organization, agenda, meeting minutes, attendance sheet.
Qualifications
  • PhD (preferred) in Biomedical Engineering or science or medical related field, clinical trials, or related field.
  • Bachelor's degree in science or medical related field, clinical trials, or related field.
  • Prior experience with clinical trials is a plus (clinical research associates are welcome to apply).
  • Prior experience as a Project Coordinator within a CRO or a pharma company is preferred.
  • Knowledge of Medical Imaging desirable but not mandatory.
  • Understanding of International Conference on Harmonization (ICH)-Good Clinical Practice (GCP) guidelines and other regulatory requirements that may impact clinical trials (FDA, EMA, etc.).
  • Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
  • Very good level of English; should be able to communicate fluently and write documents.
  • Good organizational and communication skills.

No travel required.

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

  • Flexible work environment.
  • Competitive compensation and benefits package.
  • Competitive PTO packages.
  • Structured career paths with opportunities for professional growth.
  • Company-sponsored employee appreciation events.
  • Employee health and wellness initiatives.

Awards

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
  • 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

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