We are looking for a Senior Biostatistician to join our team!

The Senior Biostatistician is a core member of the Biostatistics & Statistical Programming group who is able to lead teams, provide sound statistical guidance and consultation on both academic and regulatory directed initiatives.

In this position you will:

  • Guide project teams in study design and statistical analysis as well as communicate and confidently interact with project team members and clients.
  • Provide statistical input on clinical electronic data capture (EDC) design and edit checks.
  • Provide statistical leadership for the design, writing and review of study protocols, including the design of studies and sample size/power estimations.

Lead the development and review of statistical analysis plans (SAP)

  • Utilize SAS for programming, validation, analysis, and reporting of clinical data (proficiency in other statistical or programming languages e.g. R, Python is welcome).
  • Analyze data for, and prepare and review interim study reports, manuscripts, abstracts, and grants.
  • Provide general statistical support and consulting services.
  • Ensure compliance with GCP, FDA, and ICH guidelines and CPC standards.
  • Effectively communicate statistical issues to project team members to influence team decisions.

Here’s what you will need to bring to the table:

  • Master’s or Ph.D. degree in biostatistics or related field
  • Minimum of 5 years of experience in the analysis of data for clinical trials
  • Ability to work with minimal supervision
  • Demonstrable programming experience with SAS 9.0 or higher in a Windows environment
  • Ability to work as a member of a team
  • Strong communication skills as you may oversee others in the development or validation of statistical programming
  • Experience with MS Office Suite (Word, Excel, PowerPoint, Outlook)
  • Good knowledge of ICH guidelines, experience with Phase I-III clinical trials and FDA/NDA submissions
  • Impeccable attention to detail
  • Excellent analytical and organizational skills
  • Leadership ability to serve as a lead biostatistician on project teams

Note: Viable applicants will be required to demonstrate their computer skills as well as pass a background check.

This is not a remote position; employee will work the majority of time in the office in a team environment.

Please include a short cover letter with answers to the following questions:

  • Why would you be a good candidate for this position?
  • How many years of experience in the analysis of data for clinical trials do you have?
  • Any gaps in your employment history? Please explain.
  • What are your salary expectations?
  • Do you have a Master’s or Ph.D. degree in biostatistics or related field?
  • Are you authorized to work in the United States?
  • Do you now or will you in the future require sponsorship for employment visa status (e.g., H-1B visa status)?

CPC offers a comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)