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Medpace Reference Laboratories is a global, full-service central clinical trial laboratory specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 80 countries across the globe. Medpace has established laboratories in the USA, Europe, Singapore, and China. Our services continue to expand, with the introduction of new laboratory capabilities in all our global laboratories.Medpace Reference Laboratories is a full service central clinical trial laboratory offering project management, laboratory services, data management, logistics, and sample management and archiving capabilities, and quality assurance.
Medpace Reference Laboratories (MRL) is currently seeking a full-time Project Coordinator to join our offices in Leuven, Belgium.
Responsibilities
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
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Medpace Reference Laboratories (MRL) is currently seeking a full-time Project Coordinator to join our offices in Leuven, Belgium.
Responsibilities
- Maintain study-related documents;
- Attending study team calls;
- Primary point of contact for study teams and investigational sites;
- Preparing study metrics;
- Ensure that all aspects of designated clinical protocol are in accordance with project timelines, budgets and performance quality;
- Coordinate laboratory shipments;
- Compose and maintain departmental operating procedures and work instructions; and
- Interact with Project Managers, Sponsors, and vendors on project-related issues.
- Min. Bachelor's degree in life sciences (e.g. Biomedical Sciences)
- Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
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
- 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
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Key Skills
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- Posted
- Jun 23, 2025
- Type
- Full-time
- Level
- Not Applicable
- Location
- Leuven
- Company
- Medpace
Industries
Pharmaceutical Manufacturing
Categories
Other
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