Job Description
A Princeton based CRO is looking for a Project Statistician to join their team
Responsibilities:
* Generating statistical output for Phase I clinical studies
* Develop statistical analysis plans
* SAS programming activities
* Creation and validation of statistical tables and data listing
* Providing statistical contributions to study protocols and study reports
* Provide statistical review and input for study protocol design
* Review of case report forms prior to finalization
* Develop statistical analysis plans
* Generate research subject randomization schedules
* Create adn validate statistical tables and data listings
* Generate statistical output for Phase I clinical studies
* Generate pharmacokinetic output using WinNonlin
* Prepare statistical contributions to study reports
Job Requirements
Requirements
* BS of MS in Statistics or a related discipline with a concentration on statistics is required
* At least 5 years of experience as a statistician for clinical studies in CROs and/or
biopharmaceutical companies (prior CRO experience extremely important)
* Knowledge of drug development and study design
* Must be proficient in SAS programming and computer skills (i.e. word processing, spreadsheets, and scientific graphing software)
* Good communication skills
* Experience with WinNonlin a plus
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