Katalyst CRO
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Principal SAS Programmer
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Katalyst CRO . This role involves: 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. Creating clear and informative graphs and tables to effectively communicate PK/PD findings. Ensuring CDISC compliance and formatting data according to CDISC standards for regulatory submissions. Performing validation checks on programming code and analysis results to maintain data integrity. Identifying problems and developing tools to increase the efficiency and capacity of the Clinical PK/PD Programming group. Providing training to fellow programmers on industry guidance and software features. Responsibilities include: Data preparation and cleaning. PK/PD analysis programming. Data visualization and reporting. Requirements: Bachelor's degree in Math, Stats, Computer Science, or similar. 7+ years of industrial experience. Advanced SAS programming skills; knowledge of R is beneficial. Knowledge of CDISC standards (SEND, SDTM, ADaM). Experience with data visualization and presentation. Ability to implement advanced modeling and statistical procedures. Strong understanding of clinical trial data and hands-on data manipulation skills. Professional attitude, attention to detail, organizational skills, and effective communication. Additional details: Senior level: Mid-Senior level. Employment type: Contract. Job function: Information Technology. Industry: Pharmaceutical Manufacturing. This job posting is active and not expired. #J-18808-Ljbffr
Principal SAS Programmer
role at
Katalyst CRO . This role involves: 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. Creating clear and informative graphs and tables to effectively communicate PK/PD findings. Ensuring CDISC compliance and formatting data according to CDISC standards for regulatory submissions. Performing validation checks on programming code and analysis results to maintain data integrity. Identifying problems and developing tools to increase the efficiency and capacity of the Clinical PK/PD Programming group. Providing training to fellow programmers on industry guidance and software features. Responsibilities include: Data preparation and cleaning. PK/PD analysis programming. Data visualization and reporting. Requirements: Bachelor's degree in Math, Stats, Computer Science, or similar. 7+ years of industrial experience. Advanced SAS programming skills; knowledge of R is beneficial. Knowledge of CDISC standards (SEND, SDTM, ADaM). Experience with data visualization and presentation. Ability to implement advanced modeling and statistical procedures. Strong understanding of clinical trial data and hands-on data manipulation skills. Professional attitude, attention to detail, organizational skills, and effective communication. Additional details: Senior level: Mid-Senior level. Employment type: Contract. Job function: Information Technology. Industry: Pharmaceutical Manufacturing. This job posting is active and not expired. #J-18808-Ljbffr