Current jobs related to Sr SAS Programmer - Irvine - Katalyst CRO

  • Sr SAS Programmer

    7 days ago

    Irvine, United States Katalyst HealthCares & Life Sciences Full time

    Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (, CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following. To support the Biostatistics team by carrying out programming...

  • Sr. SAS Programmer

    6 days ago

    Irvine, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group,...

  • Sr SAS Programmer

    2 weeks ago

    Irvine, CA, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following. To support the Biostatistics team by carrying out...

  • Sr SAS Programmer

    3 days ago

    Irvine, CA, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following. To support the Biostatistics team by carrying out...

  • Sr SAS Programmer

    2 weeks ago

    Irvine, CA, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following. To support the Biostatistics team by carrying out...

  • Sr. SAS Programmer

    1 day ago

    Irvine, CA, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics...

  • Sr. Statistical Programmer

    3 weeks ago

    Irvine, United States Katalyst HealthCares & Life Sciences Full time

    Senior SAS Programmer / Statistical SAS Programmer Responsibilities: The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming support for clinical trials and contributing to the development of departmental standards. This includes developing and validating SAS programs for statistical tables, data listings, figures, and...

  • Sr. Statistical Programmer

    1 week ago

    Irvine, CA, United States Katalyst HealthCares & Life Sciences Full time

    Senior SAS Programmer / Statistical SAS Programmer Responsibilities: The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming support for clinical trials and contributing to the development of departmental standards. This includes developing and validating SAS programs for statistical tables, data listings, figures, and...

  • Senior Statistical Programmer

    2 weeks ago

    Irvine, United States Johnson & Johnson MedTech Full time

    A leading healthcare technology company is seeking a Senior Statistical Programmer in Irvine, California. This role involves developing analysis datasets and statistical programming for clinical trials, utilizing SAS and R. Ideal candidates will have a Bachelor’s degree in a relevant field and a minimum of 4 years experience in clinical research, along...

  • Senior Statistical Programmer

    3 weeks ago

    Irvine, United States Katalyst HealthCares & Life Sciences Full time

    Senior SAS Programmer / Statistical SAS Programmer Responsibilities: The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming support for clinical trials and contributing to the development of departmental standards. This includes developing and validating SAS programs for statistical tables, data listings, figures, and...

Sr SAS Programmer

4 weeks ago

Irvine, United States Katalyst CRO Full time

Join to apply for the Sr SAS Programmer role at Katalyst CRO 2 days ago Be among the first 25 applicants Responsibilities Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following. To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment area: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g., publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors to develop or monitor the content and structure of SAS data sets. Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Maintaining standards for programming activities. Working independently to accomplish tasks and goals defined by supervisor. Requirements Minimum of bachelor's degree in related science discipline. Minimum 6+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Experience in CDISC data standards, e.g. SDTM and ADaM. Proven experience with Unix and Windows operating systems. Understanding of the software development life cycle. Understanding of FDA guidelines. Good organization, time management, and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. Applies good judgment and demonstrates initiative to resolve issues. Seniority level Mid-Senior level Employment type Contract Job function Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x #J-18808-Ljbffr