Join to apply for the Principal SAS Programmer role at Katalyst CRO Responsibilities Data preparation and cleaning. Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis. Programming PK/PD analyses. Writing SAS code to perform descriptive analysis of PK/PD data and statistical analysis of exposure-response relationships. Data visualization. Creating clear and informative graphs and tables to effectively communicate PK/PD findings. CDISC compliance. Ensuring data is formatted according to CDISC standards for regulatory submissions. Validation and quality control. Performing thorough validation checks on programming code and analysis results to maintain data integrity. Identifies problems and develops tools that increase the efficiency and capacity of the Clinical PK/PD Programming group. Providing training to fellow programmers on industry guidances, new or enhanced features of software tools relevant to the role. Requirements Bachelor's degree in Stats, Computer Science, or a related life sciences field. 7+ years of industrial experience. Advanced SAS programming skills; knowledge of R is beneficial. Knowledge of CDISC standards (SEND, SDTM, ADaM). Experience visualizing and presenting data for stakeholders or clients. Ability to implement advanced modeling and statistical procedures. Strong understanding of clinical trial data, data manipulations, analysis, and reporting. Handling of uncleaned data and data issues. Professional attitude, self-motivated, with logical thinking. Excellent attention to detail and organizational skills. Effective communication and interpersonal skills. Problem-solving skills and a drive to learn new techniques and technologies. #J-18808-Ljbffr Katalyst CRO
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