Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach.
We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries.
Program study analyses and review study results; and
Communicate the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis.
Industry working experience with SAS programming, or SAS certificate
Knowledge of databases and data management process; and
Knowledge of statistical methods commonly used in pharmaceutical clinical trials.
When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices.
Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.