Katalyst Healthcares & Life Sciences Inc: Sr. SAS Programmer (PT)

Programmer is needed in United States.

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Client: Katalyst Healthcares & Life Sciences Inc

Location: Remote

Contract: Part Time

Responsibilities:

• Understanding of clinical trial objectives, design, endpoints, and procedures defined in Protocol and Statistical Analysis Plan (SAP).
• Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros.
• Collaborate with manager and other programmers through participation in formal and ad-hoc meetings.
• Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for regulatory submissions.
• Independently program CDSIC ADaM / ADS datasets and Tables Listings and figures (TLFs) as per requirement of study including efficacy related outputs.
• Provide validation support to create ADS or SDTM+, SDTM and ADaM datasets and TLFs & documentation as per the specifications within set timelines.
• Program data displays (tables, listings, graphs) for inclusion in documents including publications, statistical reports, clinical study reports, and other regulatory documents, as required.
• Independently develop QC programs to validate peer programmers’ ADS / SDTM, ADaM datasets and statistical tables, listings, and graphs.

Requirements:

• Demonstrate proficiency of programming skills. Must have experience of efficacy programming.
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Strong Base SAS v9.2 or later; SAS-STAT, and SAS Macro experience.
• Ability to work on multiple tasks and prioritize tasks.
• Excellent analytical, problem-solving, organizational, time management, interpersonal and communication skills.
• Bachelor’s degree in computer science, Statistics, Engineering or related field with minimum 4 years of related experience.
• Required skills: Create ADS /ADAM datasets from RAW / SDTM datasets according to project / CDISC analysis data model standards; Independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS datasets, spreadsheets, data listings, tables and graphical displays of clinical trials data.
• Prior experience working with Data Management on edit checks etc is preferred Good knowledge of statistical programming languages (including SAS).