What are the responsibilities and job description for the Clinical SAS Programmer position at Katalyst CRO?
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.
- A master's or bachelor's degree (or equivalent qualification) in a relevant field.
- At least 4 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.