Experienced Clinical Database Programmer

Job title:

Experienced Clinical Database Programmer

Company:

Medpace

Job description

Job SummaryOur global business is growing rapidly, and we are currently seeking a full-time office-based Clinical Database Programmer to join our Data Management team in our Leuven office. This position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. The role requires the ability to work independently and to take initiative in managing delivery timelines. This position plays a critical role on our study teams and a quality, timely database development is instrumental to the company’s and study’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

• Participate in the development, maintenance and compliance of database builds and Electronic Data Capture (EDC) standards in support of clinical studies, including but not limited to Edit Checks and CRF modules;
• Act as a resource for database issues and provide problem-solving with clinical database technology, capabilities and functionality;
• Recommend process improvements leading to more efficient and timely database builds and post-production changes;
• Gain and strengthen knowledge in multiple electronic data capture systems;
• Be an active part in multiple global project teams and collaborate with internal team members

Qualifications

• Bachelor’s degree in computer science, mathematical science, life science, or related field;
• 2+ years of programming experience;
• 1+ years of programming experience in Medidata Rave in the clinical research environment preferred, but not required;
• C#, or similar, programming experience preferred, but not required;
• Flexible and able to support a variety of studies;
• Ability to act independently and with initiative

Medpace OverviewMedpace 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.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 NextA 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

Expected salary

Location

Louvain, Brabant Flamand

Job date

Fri, 13 Sep 2024 22:24:43 GMT

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