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2017-43631

2017-43631

Title 
Biostatistician I
Job Locations 
-
US-KS-Lenexa
Posted Date 
12/8/2017

More information about this job

Overview

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.

Responsibilities

•    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.

Qualifications

  • 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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