Company:
Katalyst Healthcares & Life Sciences
Location: Houston
Closing Date: 29/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities:
Perform SAS programming activities to meet timelines, budget, and quality in accordance with Company study contracts and SOPs
Effectively 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 needs
Work with data managers to generate ongoing outputs to support data cleaning and to enhance data integrity
Communicate effectively within Biometrics and with cross-functional team members
Work on special projects as needed
Support 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 data
Good working knowledge of CDISC SDTM and ADaM Implementation Guidelines
General knowledge of regulatory requirements and drug development process
Strong verbal and written communication skills
Ability to work independently as well as part of programming teams
Strong communication skill set with peers and other group partners
Consistently 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 SOPs
Effectively 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 needs
Work with data managers to generate ongoing outputs to support data cleaning and to enhance data integrity
Communicate effectively within Biometrics and with cross-functional team members
Work on special projects as needed
Support 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 data
Good working knowledge of CDISC SDTM and ADaM Implementation Guidelines
General knowledge of regulatory requirements and drug development process
Strong verbal and written communication skills
Ability to work independently as well as part of programming teams
Strong communication skill set with peers and other group partners
Consistently deliver high quality deliverables on time and meet the project delivery expectations
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