Biostatistician III

Duration: 3 Months

Job Responsibility:

• Responsible for overseeing all aspects of statistical planning and analyses for clinical programs; directs both internal and external SAS programming efforts related to the responsible clinical programs.
• MA or Ph.D. in (Bio) statistics. Requires 5 to 7 years of experience in pharmaceutical or biotechnology industry.
• Must have experience preparing analysis programs for clinical trials phases I-III.
• Must have been primary statistician on at least one NDA/BLA.
• Must have sound knowledge of statistical applications for clinical trials.
• Excellent writing and communication skills, and knowledge and skills of programming important.
• Strong knowledge of and experience in clinical trials design.
• Very good knowledge of drug development regulations pertinent to trial design and statistical analysis.

• Proficiency in R, SAS, and/or Python, with demonstrated expertise in developing, validating, and implementing statistical analyses and simulation studies, such as ANCOVA, multiple imputation (MI), multiplicity control (type I error control, power calculation).
• Solid understanding of statistical theory and hands-on experience with statistical computing, simulations, and data interpretation
• Ability to independently lead statistical activities and also work in a collaborative environment.

• Master or PhD in Statistics or Biostatistics (PhD preferred)