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Statistics 🏢 Full Time ⭐️ Verified

Senior Statistician (Clinical Trials)

StatQuest Analytics
Boston, MA
Salary Estimate
USD 120.000 – USD 180.000
Posting Time
7 Mei 2026
Deadline
7 Mei 2027

Job description

StatQuest Analytics is seeking a Senior Statistician to lead analyses in clinical trials and health research. This full-time role is based in Boston, MA with hybrid work options.

In this role, you will partner with biostatisticians, data managers, and scientists to design robust analyses, pre-specify statistical methods, and ensure regulatory readiness for submissions. You will translate complex statistical results into actionable insights for cross-functional teams.

We offer a competitive compensation package, comprehensive benefits, and a culture that values curiosity, rigor, and collaboration.

Responsibility

  • Lead the development of statistical analysis plans for Phase I to III clinical trials, including sample size calculations and power analyses.
  • Execute and oversee advanced statistical analyses using R, SAS, or Python, ensuring reproducible and auditable results.
  • Collaborate with statisticians and clinical teams to interpret results and communicate findings to non-statistical audiences.
  • Pre-specify primary and secondary endpoints, adapt analysis strategies for missing data, and manage data quality checks.
  • Contribute to trial design strategy, randomization schemes, and Bayesian or frequentist approaches as appropriate.
  • Prepare statistical reports, figures, and tables for regulatory submissions and publications.
  • Mentor junior statisticians, provide technical guidance, and review code and outputs for quality control.
  • Stay current with statistical methodologies and industry regulations to maintain best practices.

Qualification

  • Master's or PhD in Statistics, Biostatistics, Mathematics, or a closely related field.
  • At least 5 years of hands-on experience in clinical trial statistics or biostatistics.
  • Proficiency in R and SAS; Python experience is a plus. Strong data visualization skills.
  • Experience with mixed effects models, survival analysis, GLMs, and interim analyses.
  • Strong understanding of regulatory guidelines (ICH GCP, CDISC) and trial reporting standards.
  • Excellent written and verbal communication abilities; ability to explain complex statistics to diverse audiences.
  • Ability to work independently and in multidisciplinary teams; project management skills.

Required Skills

Statistics R SAS Python biostatistics clinical trials experimental design data visualization linear models mixed-effects survival analysis Bayesian statistics regulatory submissions

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