Katalyst CRO
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Senior Statistical Programmer
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Katalyst CRO . This is a job posting from 7 months ago and may no longer be active. Responsibilities
Serve as a programming project lead on multiple complex studies to distribute and oversee tasks for the programming team, communicate with clients, plan and execute delivery, and manage resources and project priorities effectively. Ensure budget and scope alignment. Apply advanced knowledge of CDISC standards and electronic data submission (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer's Guide, Analysis Results Metadata). Provide expertise on regulatory submission requirements. Lead department process improvement projects, including development of standard SAS Macros and programming standards. Train and coach Statistical Programmers, Biostatisticians, and other departments on processes, tools, and collaboration roles. Requirements
Master's or bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science with strong programming experience. Attention to detail, problem-solving skills, organizational and interpersonal communication skills. 8+ years of SAS programming experience in CRO, Pharma, Biotech, or Healthcare industries. Knowledge of statistics and analytical skills. Focus on quality, accuracy, and completeness. Excellent communication skills. Understanding of Good Clinical Practice. Ability to lead, estimate scope, handle resources, and meet project timelines. Additional Details
Seniority level: Mid-Senior level Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting may be expired or no longer accepting applications. #J-18808-Ljbffr
Senior Statistical Programmer
role at
Katalyst CRO . This is a job posting from 7 months ago and may no longer be active. Responsibilities
Serve as a programming project lead on multiple complex studies to distribute and oversee tasks for the programming team, communicate with clients, plan and execute delivery, and manage resources and project priorities effectively. Ensure budget and scope alignment. Apply advanced knowledge of CDISC standards and electronic data submission (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer's Guide, Analysis Results Metadata). Provide expertise on regulatory submission requirements. Lead department process improvement projects, including development of standard SAS Macros and programming standards. Train and coach Statistical Programmers, Biostatisticians, and other departments on processes, tools, and collaboration roles. Requirements
Master's or bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science with strong programming experience. Attention to detail, problem-solving skills, organizational and interpersonal communication skills. 8+ years of SAS programming experience in CRO, Pharma, Biotech, or Healthcare industries. Knowledge of statistics and analytical skills. Focus on quality, accuracy, and completeness. Excellent communication skills. Understanding of Good Clinical Practice. Ability to lead, estimate scope, handle resources, and meet project timelines. Additional Details
Seniority level: Mid-Senior level Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting may be expired or no longer accepting applications. #J-18808-Ljbffr