Medpace, Inc
80339 Munich, Germany
Job Description
employment type
full time
Full job description
Responsibilities :
Write statistical programs for use in creating analysis datasets, tables, listings, and figures;
Review analysis plans for appropriate methods;
Program study analyzes and review study results; other
Communicate the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis.
Qualifications :
Master's Degree in Statistics/Biostatistics required
SAS and/or statistical programming experience;
Knowledge of databases and data management process; other
Knowledge of statistical methods commonly used in pharmaceutical clinical trials.
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...