Katalyst CRO
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Principal Statistical Programmer
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Katalyst CRO . Responsibilities include: Perform SAS programming activities to meet timelines, budget, and quality standards in accordance with company study contracts and SOPs. Collaborate effectively with Biostatisticians and the Statistical Programming team to review data specifications, generate or QC analysis datasets, and produce or QC analysis outputs for internal medical monitoring, CSR, and submission needs. Work with data managers to generate ongoing outputs supporting data cleaning and enhancing data integrity. Communicate effectively within Biometrics and with cross-functional teams. Work on special projects as needed. Support internal analysis data and reporting deliverables, ensuring timely, targeted, and accurate reporting and outcomes. Requirements include: Bachelor's Degree in statistics, computer science, or related field with at least 5 years of SAS programming experience in clinical trials, or master's degree with at least 8 years of experience. Good knowledge of CDISC SDTM and ADaM guidelines. Understanding of regulatory requirements and drug development processes. Strong verbal and written communication skills. Ability to work independently and as part of a team. Consistently deliver high-quality work on time. Additional details: Seniority level: Associate Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting is active and not expired. #J-18808-Ljbffr
Principal Statistical Programmer
role at
Katalyst CRO . Responsibilities include: Perform SAS programming activities to meet timelines, budget, and quality standards in accordance with company study contracts and SOPs. Collaborate effectively with Biostatisticians and the Statistical Programming team to review data specifications, generate or QC analysis datasets, and produce or QC analysis outputs for internal medical monitoring, CSR, and submission needs. Work with data managers to generate ongoing outputs supporting data cleaning and enhancing data integrity. Communicate effectively within Biometrics and with cross-functional teams. Work on special projects as needed. Support internal analysis data and reporting deliverables, ensuring timely, targeted, and accurate reporting and outcomes. Requirements include: Bachelor's Degree in statistics, computer science, or related field with at least 5 years of SAS programming experience in clinical trials, or master's degree with at least 8 years of experience. Good knowledge of CDISC SDTM and ADaM guidelines. Understanding of regulatory requirements and drug development processes. Strong verbal and written communication skills. Ability to work independently and as part of a team. Consistently deliver high-quality work on time. Additional details: Seniority level: Associate Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting is active and not expired. #J-18808-Ljbffr