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Veristat

Biostatistician II

Veristat

. Perform analysis of clinical trial data .

Posted 10/5/2026full-timeRemote • CanadaMid-LevelSenior💰 $92,000 - $107,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in statistical analysis and biostatistics, particularly in the context of Phase I-IV clinical trials. Proficient in SAS and Microsoft Office tools, with strong communication skills and the ability to manage multiple tasks effectively under tight deadlines.

Highest-signal resume keywords
PhD In Statistics Or BiostatisticsSAS Proficiency Including BASE And STATStatistical Methods For Phase I-IV Clinical TrialsBiostatistical Experience In Clinical TrialsExcellent Written And Oral Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Statistical AnalysisBiostatisticsStatistical MethodsClinical Trial Data AnalysisTechnical Writing
Soft Skills
Detail OrientationTime Management
Tools & Technologies
SASMicrosoft WordMicrosoft Excel
Industry Keywords
Clinical TrialsHealth ResearchPhase I-IV Trials

About the role

Key responsibilities & impact
  • Perform analysis of clinical trial data
  • Provide statistical input into reporting of clinical trial results
  • Work largely independently with minimal oversight from the Director or Manager of Biostatistics, or Senior Biostatistician
  • Apply statistical methods to Phase I-IV clinical trials
  • Manage multiple tasks under tight timelines

Requirements

What you’ll need
  • PhD degree in Statistics, Biostatistics, or related field with relevant academic experience OR a Master’s degree in Statistics or Biostatistics or a related field and 3 years of biostatistical experience in the clinical trials or health research environment OR a Bachelor’s degree in Statistics, Biostatistics or a related field and 5 years of biostatistical experience in a clinical research organization in a hands-on technical position with a demonstrated ability to perform the duties above
  • Excellent written and oral communication skills including grammatical/technical writing skills
  • Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
  • SAS proficiency including BASE and STAT; GRAPH preferred
  • Proficiency in Microsoft Word and Excel
  • Strong level of detail orientation
  • Ability to work on multiple tasks under tight timelines

Benefits

Comp & perks
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans
  • Applicable bonus