Veristat
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. What You Will Do
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. What We Offer
Remote working Flexible time off Paid holidays Medical insurance Tuition reimbursement Retirement plans What We Look For
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.
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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. What You Will Do
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. What We Offer
Remote working Flexible time off Paid holidays Medical insurance Tuition reimbursement Retirement plans What We Look For
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.
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