Senior SAS Programmer

PVR Technologies, Inc,   King Of Prussia, PA   Full-time     Information Services / Technology (IT)
Posted on July 23, 2022

Senior SAS Programmer

Duties: Lead statistical programming activities for phase I to IV clinical studies & co-ordinate programming activities within study/project; Manage & lead statistical programming team with delivery of Clinical Study Report (CSR) through both internal & external delivery models using applicable data standards and regulations; Ensure quality control (QC) on all process & technical activities related to derived dataset, table, listing, and figure programming in accordance with corporate quality standards; Design & develop programming algorithms in R, R shiny, and its ecosystem, & provide analytical support to statisticians & statistical programmers; Create DOS batch script/UNIX shell scripts to automate & schedule SAS program to execute and secure programs and/or data dependencies; Create and validate analysis datasets such as ADSL, ADRS, ADTTE, ADEFF, ADAE, ADEX, ADVX, etc; Develop variables such as TRTP, TRTPN, TRTA, APERIOD, APERIODC, APEREDT, APERETM for BDS and OCCDS datasets using programming tools & skills; Apply statistical modeling skills & utilize Regression Model to examine, analyze relationship between variables in clinical trials; Lead and manage statistical programming with to produce Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Report (PBRER), Investigator’s brochures (IB); Use statistical software like Spotfire & data visualization tools such as Tableau to create & maintain listings, tabulations, graphical summaries, and formal statistical estimates and tests.

Skills: R, R shiny, SAS program , UNIX shell scripts, Spotfire, data visualization & Tableau. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US. 

Requirements: Master’s degree in Health Services Administration, Public Health with 2 years of experience in a job title with similar duties and skills.