[Remote] Principal Biostatistician
Note: The job is a remote job and is open to candidates in USA. Veristat is a global team with over 30 years of expertise in accelerating life-changing therapies to patients worldwide. The Principal Biostatistician provides statistical input into Phase I - IV clinical trial development, analyzes clinical trial data, and serves as a lead statistician on clinical trials.
Responsibilities
ā¢ Provides statistical input into Phase I - IV clinical trial development
ā¢ Performs the analysis of clinical trial data
ā¢ Provides statistical input into the reporting of clinical trial results
ā¢ Can work independently and function as a lead statistician on clinical trials
Skills
ā¢ 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
ā¢ 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
ā¢ Familiarity with SAS, SPSS or other statistical software package
ā¢ Proficiency in Microsoft Word and Excel
ā¢ Strong level of detail orientation
ā¢ Ability to work on multiple tasks under tight timelines
Benefits
ā¢ Remote working
ā¢ Flexible time off
ā¢ Paid holidays
ā¢ Medical insurance
ā¢ Tuition reimbursement
ā¢ Retirement plans
Company Overview
ā¢ Veristat is a full service Clinical Research Organization (CRO). It was founded in 1994, and is headquartered in London, England, GBR, with a workforce of 501-1000 employees. Its website is http://www.veristat.com.
Company H1B Sponsorship
ā¢ Veristat has a track record of offering H1B sponsorships, with 2 in 2025, 1 in 2024, 2 in 2023, 5 in 2022, 2 in 2021, 11 in 2020. Please note that this does not guarantee sponsorship for this specific role.
Apply Now
Apply Now
Responsibilities
ā¢ Provides statistical input into Phase I - IV clinical trial development
ā¢ Performs the analysis of clinical trial data
ā¢ Provides statistical input into the reporting of clinical trial results
ā¢ Can work independently and function as a lead statistician on clinical trials
Skills
ā¢ 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
ā¢ 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
ā¢ Familiarity with SAS, SPSS or other statistical software package
ā¢ Proficiency in Microsoft Word and Excel
ā¢ Strong level of detail orientation
ā¢ Ability to work on multiple tasks under tight timelines
Benefits
ā¢ Remote working
ā¢ Flexible time off
ā¢ Paid holidays
ā¢ Medical insurance
ā¢ Tuition reimbursement
ā¢ Retirement plans
Company Overview
ā¢ Veristat is a full service Clinical Research Organization (CRO). It was founded in 1994, and is headquartered in London, England, GBR, with a workforce of 501-1000 employees. Its website is http://www.veristat.com.
Company H1B Sponsorship
ā¢ Veristat has a track record of offering H1B sponsorships, with 2 in 2025, 1 in 2024, 2 in 2023, 5 in 2022, 2 in 2021, 11 in 2020. Please note that this does not guarantee sponsorship for this specific role.
Apply Now
Apply Now