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2018-44804

2018-44804

Title 
Sr Biostatistician (Titusville, NJ)
Job Locations 
-
US-NJ
US-PA
US-NY
Posted Date 
2/16/2018

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

  • 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.

Qualifications

  • 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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