Biostatistician

ProPharmaWindsor, QC
Remote

About The Position

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Requirements

  • In-depth knowledge of statistical methodologies.
  • Excellent Communication and interpersonal skills, with the ability to work collaboratively in cross functional teams and with external partners.
  • Ability to program in SAS and or R.
  • M.S. in Biostatistics.
  • None

Responsibilities

  • Support statistical activities for clinical trials and data analyses, including study design, statistical analysis plan development, and statistical analysis.
  • Ensure the quality and accuracy of statistical deliverables, including statistical reports, tables, listings, and figures.
  • Assist in the development and review of clinical study protocols and case report forms (CRFs) to ensure appropriate statistical analysis.
  • Develop and maintain SAS programs for statistical analysis in accordance with standard operating procedures (SOPs), good programming practices, and regulatory guidelines.
  • Other duties as assigned.
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