Clinical Project Coordinator (CRO)

☞ Medpace

Visualizza: 135

Giorno di aggiornamento: 29-11-2025

Località: Leuven Flemish Brabant

Categoria: Pianificazione / Progetti IT - Software

Industria: Pharmaceutical Manufacturing

Posizione: Mid-Senior level

Tipo di lavoro: Full-time

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Contenuto del lavoro

Our clinical activities are growing rapidly in Belgium, and we are currently seeking a full-time Project Coordinator to join our Clinical Operations team. This position will work on 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.

As a paid, full-time project coordinator you will have the opportunity to work within Clinical Trial Management, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Clinical Trial Managers, you will gain valuable hands on experience to enable you to develop a career in clinical research.

Responsibilities

  • Provide day-to-day departmental/project support activities, such as maintenance of project-related files and faxing documents to sites;
  • Coordinate and provide minutes for department/project meetings or conference calls;
  • Conduct quality control of documents;
  • Maintain spreadsheets and compile reports; and
  • Perform other tasks as needed.

Qualifications

  • Master or/and PhD degree is required (preferably in a Life Sciences field);
  • Some experience in an office setting is preferred;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office;
  • Great attention to detail and excellent oral and written communication skills; and
  • Preferred: Dutch & French language skills and fluency spoken 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?

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
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Scadenza: 13-01-2026

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