Clinical Research

• Providing statistical support to clinical studies, with a focus on Rare Disease;
• Participating in the development of study protocols, including participation in study design discussions and sample size calculations;
• Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications;
• Performing statistical analyses;
• Interpreting statistical results;
• Preparing clinical study reports, including integrated summaries for submissions;
• Leading study activities when called upon;
• Utilizing your strong communication skills to present and explain methodology and consequences of decisions in lay terms;
• Serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.

Principal Biostatistician, FSP

Clinical Trial Manager I

Head and Neck Clinical Research Coordinator

Clinical Research Coordinator I – Non RN

Senior Clinical Study Manager