Associate Director, Biostatistician (Park Ridge, NJ)
-Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.
-Work with the clinical study team on study design, development and/or review of clinical study protocols.
-Develop and/or review statistical analysis plans, including Table/listing/figure shells, and final study report for clinical studies; perform post-hoc statistical analyses as needed.
-Work with the project statistician and clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality.
-Oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, ensure the quality of CRO deliverables.
-MS or PhD in Biostatistics/Statistics with at least 7 years of experience in the pharmaceutical, CRO or biotech industry or research institute
-Strong SAS programming skills.
-Neuroscience experience is preferred. PhD is preferred.