Designs, plans, and executes biostatistical components of clinical trials. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.
• Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies. • Serves as an independent reporting statistician on data monitoring committees. • Develops statistical analysis plans and reporting specifications for simple to complex clinical studies. • Reviews statistical analyses of other statisticians and interprets results from simple to complex clinical studies. • Performs senior review of TFLs and statistical analysis plans. • Provides significant input in the development and review of CRFs, edit specifications, and critical variable lists. • Performs lead review of TFLs and derived datasets for clinical studies. • Contributes to clinical study protocols and clinical study reports. • Reviews simple to complex randomization specifications and dummy randomization schemes. • Trains and mentors new or junior statisticians on statistical methods and PRA procedures. • Provides statistical training at monthly seminars. • Participates in bid defense meetings.
8 years of biostatistical experience
Master’s degree in statistics or biostatistics
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.