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Sr Biostatistician (Titusville, NJ)
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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.


  • Acts as a Lead Statistician on simple to complex individual studies.
  • Acts as a Lead Statistician on simple submissions.  
  • Acts as an unblinded statistician on simple to moderate studies.
  • Able to represent client at regulatory agency meetings in association with simple studies.
  • Looks to develop client contacts and provide new leads for business development.
  • Provides statistical services to clients and internal colleagues on statistical issues at a simple to complex level.
  • Contributes to process improvement and statistical working groups.
  • Contributes to internal training and discussions of statistical methodologies.
  • Provides senior reviews and oversight of more junior statisticians.
  • Exhibits good knowledge of multiple statistical and therapeutic areas, the drug development process, SAS procedures, and good programming practices.
  • Demonstrates ability to plan, implement, and monitor the statistical processes for multiple clinical studies.


  • Master’s degree in statistics or biostatistics is required.
  • Minimum of 5 years of biostatistical experience in clinical trials is required.
  • Must have experience writing protocols and creating statistical analysis plans.
  • Must have experience facilitating database lock.
  • Must have experience with review of table listings, figures, and graphs.
  • Must have helped review clinical study reports and case report forms.
  • Experience with mixed models and timed event analysis, categorical data analysis is required.
  • Proficiency with SAS and/or R is required.
  • Early Phase and Late Phase experience is desired, but not required.
  • Must be able to work on-site in Titusville, New Jersey for up to 6 weeks during initial onboarding and training period. Following training period, must be able to work from Titusville, New Jersey location as needed (likely work from home 2 - 3 days/week). Potential flexibility to be discussed at time of interview. 


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


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