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We have an immediate opening for an entry-level Biostatistician. The Biostatistician may review protocols and case report forms, perform sample size calculations, write Statistical Analysis Plans, develop and produce interim and final reports. Additionally, this position will support Project Directors in the production and presentation of Data Monitoring Committee reports, analyzing data for regulatory submissions and publications, and communicating with clients and team members is desired.

Qualifications and Experience:

  • PhD or Master’s degree in biostatistics or statistics
  • 1 year experience with clinical trials is desired

Knowledge, Skills and Abilities:

  • Proficiency in statistical programming (SAS preferred)
  • Good communication skills
  • Knowledge of FDA requirements and experience in the pharmaceutical or biotechnology industries are desired

This is a full time on-site position with great career development and advancement opportunities. Candidates selected for employment must pass a background check before employment begins.



This job is not currently accepting applications!