Principal Biostatistician

Principal Biostatistician

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.

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

• 105+ approved therapies for marketing applications prepared by Veristat
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
• Learn more about our core values here!

• 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 IIV clinical trials are required.
• 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.

Automated Decision Making :
All applicants are reviewed by a member of the Veristat Talent Acquisition team;
Veristat does not utilize an automated decision‑making process.

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