My client is a vaccine Biotechnology company in the Gaithersburg MD area
You will be responsible for the design, analysis, and reporting of clinical trials. This position involves interaction with Contract Research Organizations (CROs), as well as Medical Affairs, Data Management, Clinical Scientists and Regulatory Affairs in designing and analyzing clinical trials and coordinating the statistical activities for drug development projects. Additionally, this position provides statistical support to publications by performing statistical analyses of clinical trial data.
MS with 7+ years, or PhD with 5+ years of related work experience working for biotech, pharma or CRO
Experience with SAS programming
Experience with large molecule projects