Job Summary :
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.
What to Expect Next
Our global business is growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team in our Leuven office. The position will work in a team to develop databases in which clinical data is captured and processed for analysis and reporting. This position plays a critical role within our study teams and ensuring quality, timely database development is instrumental to the company’s success. If you are interested in an exciting career where you have the opportunity to use your knowledge and expertise and can develop and grow your career even further, then this is the position for you!
Responsibilities :
- Communicate with internal teams at Medpace Reference Laboratories (MRL) regarding study progress;
- Work closely with the Project Management team to setup, validate, and maintain study databases according to sponsor specifications;
- Programming responsibilities entail using syntax built specifically for MRL to build custom expressions that meet specific sponsor requests.
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Act as the primary data management contact for ongoing projects, which includes:
- Supplying technical support to internal Medpace personnel;
- Ensuring quality of the database build;
- Following up on the progress of projects to ensure sponsor timeline expectations are met.
- Bachelor’s degree in computer science, mathematical science, life science or related field;
- Knowledge of Microsoft Office;
- An interest in programming languages is preferred;
- Knowledge of medical terminology is preferred;
- Excellent verbal and written communication skills;
- Meticulous attention to detail.
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? :
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.
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