Clinical SAS ProgrammerKatalyst HealthCares & Life Sciences • Irving, TX
Clinical SAS Programmer
Katalyst HealthCares & Life Sciences • Irving, TX
[job_card.30_days_ago]
[job_preview.job_type]
- [job_card.full_time]
[job_card.job_description]A master's or bachelor's degree (or equivalent qualification) in a relevant field. At least + years of solid experience in statistical programming with clinical trial data, particularly using SAS software. A strong team player who is open to learning and adopting new methods and technologies, contributing positively to team dynamics. A quick learner with a proven history of effective collaboration and teamwork. Exceptional communication skills, both written and verbal. Demonstrated ability to multitask, prioritize, anticipate potential challenges, and achieve goals within a multidisciplinary team environment.
Responsibilities :
- Demonstrating proficiency in CDISC, SDTM, and ADaM to support various submission activities, including IA, CSR, DSUR, and publications.
- Providing statistical programming support to generate tables, listings, and figures for assigned projects.
- Overseeing all aspects of statistical programming, working closely with statisticians to ensure timely and accurate delivery of statistical outputs.
- Creating detailed specifications for individual studies and comprehensive summaries.
- Directing and supervising CRO activities related to statistical programming, including the creation and validation of SDTM and ADaM datasets.
- Producing safety tables, efficacy tables, and lab shift tables in accordance with the SAP and mock layouts.
- Validating datasets and tables through double programming.
- Having a good understanding of oncology-specific domains is an advantage.
- Reviewing statistical analysis plans, annotated CRFs, and integrated summaries, providing thoughtful feedback.
Requirements :
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