Statistical Programmer

Minimum Requirements: Expertise in extracting, manipulating, summarizing, analyzing, and presenting data using SAS procedures. Expertise in SAS/MACRO, SQL, and SAS/BASE procedures. Expertise/experience in the use of SAS/GRAPH and Statistical procedures. Highly experienced working in Clinical data and medical dictionaries. Knowledge of relational database principles. Able to program in Linux environment. Strong understanding of clinical trials - how programming deliverables fit into the process, what types of data are collected. Data structure understanding (BDS - Basic Data Structure, CDISC SDTM, and ADaM). Able to draft programming requirements from the statistical analysis plan. Strong experience with study reporting. Previous experience using CDARS - Preferable. Preferred Masters (US) or BSc (Europe) in statistics or a related science. Role Responsibilities: Create submission-ready standard data presentations and data sets using standard coding. Create submission-ready non-standard data presentations and data sets using non-standard coding. Conduct programming activities associated with interim analysis, QC, eSub, etc. as required. Develop and run production or QC programs. Review tables/listings, edit checks output and SAS programs, specifications, and other programming documentation to ensure quality of deliverables. Write complete, concise, and unambiguous technical documents (e.g., Lists of Tables, Mock tables, code specifications, program documentation, QC plans, QC implementation). Understand and plan work to delivery timelines including allowing time for internal Pfizer QC, as appropriate. Work with supervisor and Pfizer contact to balance conflicting priorities. Provide updates and alerts to points of contact including potential slipped delivery time, planned change to resources, and quality issues or concerns. Ensure training is done before embarking on a task. Alert supervisor and Pfizer contact where skills or knowledge are not adequate for the task set - seek help. Coordinate work on multiple projects according to priorities. Suggest improvements to standard work processes and propose new software applications to improve work efficiency/quality. Support and lead efforts to implement new concepts, process improvements, and technological advances for delivering outputs. Present technical information to a non-technical audience. May be a Primary contact to Pfizer for a group of programmers all working on the same project. Project management of a study, a portfolio of studies, or submissions, managing overall day-to-day operations. Quality overview of programming activities. #J-18808-Ljbffr

Created: 2025-03-01