Katalyst Healthcares and Life Sciences
Principal Statistical Programmer
Katalyst Healthcares and Life Sciences, Houston, Texas, United States, 77246
Responsibilities:
Perform SAS programming activities to meet timelines, budget, and quality in accordance with Company study contracts and SOPsEffectively work with Biostatisticians and Statistical Programming team to review data specs, generate or QC analysis datasets and generate or QC analysis outputs per requests for internal medical monitoring, CSR and submission needsWork with data managers to generate ongoing outputs to support data cleaning and to enhance data integrityCommunicate effectively within Biometrics and with cross-functional team membersWork on special projects as neededSupport internal analysis data and reporting deliverables. Ensure timely, targeted, and accurate reporting and outcomes.Requirements:
Bachelor's Degree in statistics, computer science or another related science field with a minimum of 5 years of SAS programming experience with clinical trial data OR master's degree in statistics, computer science or another related science field with a minimum of 8 years of SAS programming experience with clinical trial dataGood working knowledge of CDISC SDTM and ADaM Implementation GuidelinesGeneral knowledge of regulatory requirements and drug development processStrong verbal and written communication skillsAbility to work independently as well as part of programming teamsStrong communication skill set with peers and other group partnersConsistently deliver high quality deliverables on time and meet the project delivery expectations
Perform SAS programming activities to meet timelines, budget, and quality in accordance with Company study contracts and SOPsEffectively work with Biostatisticians and Statistical Programming team to review data specs, generate or QC analysis datasets and generate or QC analysis outputs per requests for internal medical monitoring, CSR and submission needsWork with data managers to generate ongoing outputs to support data cleaning and to enhance data integrityCommunicate effectively within Biometrics and with cross-functional team membersWork on special projects as neededSupport internal analysis data and reporting deliverables. Ensure timely, targeted, and accurate reporting and outcomes.Requirements:
Bachelor's Degree in statistics, computer science or another related science field with a minimum of 5 years of SAS programming experience with clinical trial data OR master's degree in statistics, computer science or another related science field with a minimum of 8 years of SAS programming experience with clinical trial dataGood working knowledge of CDISC SDTM and ADaM Implementation GuidelinesGeneral knowledge of regulatory requirements and drug development processStrong verbal and written communication skillsAbility to work independently as well as part of programming teamsStrong communication skill set with peers and other group partnersConsistently deliver high quality deliverables on time and meet the project delivery expectations