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Biostatistician / Statistical SAS Programmer

Biostatistician / Statistical SAS Programmer

Ursus, Inc.San Francisco, CA, US
12 days ago
Job type
  • Full-time
Job description

JOB TITLE : Biostatistician / Statistical SAS Programmer

LOCATION : 100% Remote, EST or CST

DURATION : 12 months with possible conversion

RATE RANGE : $50-60 / hour

POSITION SUMMARY :

We are seeking a detail-oriented and technically skilled Biostatistician / Statistical SAS Programmer to support the design, analysis, and reporting of clinical and healthcare-related studies. This position requires strong statistical expertise and advanced proficiency in SAS programming to ensure the integrity and accuracy of data analysis in support of regulatory submissions and scientific publications, with a focus on cardiology medical devices.

RESPONSIBILITIES :

  • Design and analyze clinical trials and observational studies in collaboration with cross-functional teams.
  • Develop and validate SAS programs for data manipulation, statistical analysis, and report generation.
  • Create and review statistical analysis plans (SAPs), study protocols, and data specifications.
  • Perform quality control checks on datasets, tables, listings, and figures (TLFs).
  • Conduct statistical analyses using SAS and interpret results in the context of study objectives.
  • Provide statistical consultation and programming support to clinical and research teams.
  • Ensure compliance with regulatory standards (e.g., CDISC, FDA, ICH).
  • Present statistical findings to internal and external stakeholders in a clear and concise manner.
  • Stay current with advancements in statistical methodologies and SAS programming techniques.

QUALIFICATIONS :

  • Master's or PhD in Biostatistics, Statistics, or a related field.
  • Strong proficiency in SAS programming (Base, Macro, SQL, and Statistical procedures).
  • Knowledge of statistical methods such as regression, survival analysis, and mixed models.
  • Familiarity with other statistical software (e.g., R, STATA) is a plus.
  • Excellent problem-solving, communication, and teamwork skills.
  • Ability to manage multiple projects and meet tight deadlines with high attention to detail.
  • Experience with clinical trial data and regulatory submissions (e.g., CDISC SDTM / ADaM standards).

    • BENEFITS SUMMARY : Individual compensation is determined by skills, qualifications, experience, and location. Compensation details listed in this posting reflect the base hourly rate or annual salary only, unless otherwise stated. In addition to base compensation, full-time roles are eligible for Medical, Dental, Vision, Commuter and 401K benefits with company matching.

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    Biostatistician • San Francisco, CA, US