Principal Biostatistician

Overview

The Principal Biostatistician provides statistical input into Phase I - IV clinical trial development, performs the analysis of clinical trial data, and provides statistical input into the reporting of clinical trial results. The Principal Biostatistician can work independently and function as a lead statistician on clinical trials.

• Provide statistical input into Phase I - IV clinical trial development.
• Perform analysis of clinical trial data.
• Contribute to the reporting of clinical trial results and act as a lead statistician on clinical trials when needed.

• Remote working
• Flexible time off
• Paid holidays
• Medical insurance
• Tuition reimbursement
• Retirement plans

• PhD degree in Statistics, Biostatistics, or related field, and 5 years of biostatistical experience in the clinical trials or health research environment OR a Master’s degree in Statistics, Biostatistics, or related field, and 8 years of biostatistical experience in the clinical trials or health research environment.
• Excellent written and oral communication skills including grammatical/technical writing skills and familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials.
• Familiarity with SAS, SPSS or other statistical software package.
• Proficiency in Microsoft Word and Excel.
• Strong level of detail orientation.
• Ability to work on multiple tasks under tight timelines.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.