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Biostatistician I
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Designs, plans, and executes biostatistical components of clinical trials. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.


•    Serves as the lead biostatistician on project teams for simple to moderate clinical studies.
•    Develops statistical analysis plans and reporting specifications for simple to moderate clinical studies.
•    Performs statistical analyses and interprets results from simple to moderate clinical studies.
•    Participates in the development and review of CRFs, edit specifications, and critical variable lists.
•    Performs lead review of TFLs and derived datasets for clinical studies.
•    Contributes to clinical study protocols and clinical study reports.
•    Reviews simple to moderate randomization specifications and dummy randomizations.
•    Participates in bid defense meetings.


  • Master’s degree in statistics or biostatistics or a related field is required. 
  • Minimums of 3 years of biostatistical experience is required. 
  • Phase I experience is desired. But, not required. 


PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.


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