Assist in providing written statistical analysis plans and statistical sections of clinical study protocol and report for each assigned study and ensure that appropriate statistical methods are utilized; analyze data and present to internal/external groups including but not limited to clinicians and cross-functional team members; utilize technologies to collect, clean, analyze, predict, and effectively communicate information; analyze data, draw insights, and present results in a cohesive, intuitive, and simplistic manner; provide biostatistical consultation to the preparation of clinical protocols, abstracts and presentations, manuscripts for potential publication and other medical and scientific materials; participate in clinical study team meetings and provide statistical input and support to clinical trial design, conduct, data analysis, and results interpretation; and monitor conduct of clinical trials and perform quality control with respect to data to be analyzed and the programs to be used for the analysis. Master’s degree in Biostatistics or related along with proficiency in designing and modifying statistical analysis tests & methods for clinical trials to find solutions to issues relating to biology or medical research, including proficiency with R programming language through professional experience or internship. Qualified applicants please e-mail Princeton Pharmatech at jobs@princetonpharmatech.com and include job code "BIO330" in subject line.