Associate Biostatistician

Job Location US-NY-Rochester
Regular Full-Time


ERT - Rochester has an exciting new opening to join our growing team. The Associate Biostatistician is responsible for providing statistical support under the supervision of the Statisticial Operations Manager.


ERT is a global data and technology company that minimizes uncertainty and risk in clinical trials so that customers can move ahead with confidence. With nearly 50 years of clinical and therapeutic experience, ERT balances knowledge of what works with a vision for what’s next, so we can adapt without compromising standards.

Powered by the company’s EXPERT® technology platform, ERT’s solutions enhance trial oversight, enable site optimization, increase patient engagement and measure the efficacy of new clinical treatments while ensuring patient safety. Since 2014, more than half of all FDA drug approvals came from ERT-supported studies. Pharma companies, biotechs and CROs have relied on ERT solutions in 10,000+ studies spanning more than three million patients to date. By identifying trial risks before they become problems, ERT enables customers to bring clinical treatments to patients quickly — and with confidence.



  • Develop SAS and R programs for statistical analysis in conjunction with the Senior Biostatistician.
  • Test, maintain, and execute SAS and R programs to perform statistical analysis including central tendency analysis, categorical analysis, and concentration-QTc analysis for data from both TQT studies and early clinical studies, in close consultation with the Senior Biostatistician.
  • Prepare tables, figures, and listings for statistical analysis as outlined in the statistical analysis plan.
  • Assist in post-processing data activities including data QC, completing IIRV reports, and cardiologist consistency checks.
  • Perform review of final outputs and reports as it relates to the planned statistical analysis.


  • Support research programs and provide research results to the Senior Biostatistician.
  • Performing quality checks on CDISC formatted analysis datasets (ADaM). 

The duties and responsibilities listed in this job description represent the major responsibilities of the position.  Other duties and responsibilities may be assigned, as required.  ERT reserves the right to amend or change this job description to meet the needs of ERT.  This job description and any attachments do not constitute or represent a contract.





  • Master’s degree in statistics or Bachelor's degree with relevant statistics experience.


  • Minimum of one year of previous experience in statistical analysis or data analysis in clinical trials.
  • Familiarity and experience with ANOVA, t-test, regression, and linear mixed-effects modeling.
  • Computer competencies to include Microsoft Outlook, Word, and Excel.
  • Strong SAS or R programming skills
  • Ability to learn quickly, function independently, and handle increasing levels of responsibility.

The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above listed qualifications.


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