Clinical SAS / Statistical Programmer

Katalyst HealthCares & Life Sciences Inc, Indianapolis, IN (United States)

Category: Programming

Posted on: 20 Nov 2020

Job DescriptionRoles and Responsibilities:

    Support Data Management, Biostatistics and Statistical Programming activities across clinical studiesProficient in programming of clinical data using SAS softwareEnsure programs, outputs, and documentation are consistent with ICH-GCP guidelines and company SOPWrite specifications for, and generate CDISC standard SDTM and ADaM datasetsProficient in Pinnacle 21 and all eSUB required output including Define.xmlProduce summary tables, graphs, and data listings using SAS/ODSParticipate in Table, Listing and Figure shell development, annotation, and reviewDevelop standard SAS macros for efficient production of data analysis and outputValidate programs and associated output results with documentationWork with Clinical Research Organizations participating in oversight and programming activitiesProvide ad-hoc programming in support of exploratory and after-market analysisParticipate in the development and/or maintenance of departmental procedures and standardsTrain and mentor new programmers
Education and Experience:
    Bachelor's degree or higher in computer science, statistics, or equivalent8+yrs Pharma or CRO industry experience in clinical reporting and statistical applicationsAbility to work on multiple projects concurrently with strong planning and organization skillsGood communication and writing skillsAble to maintain effective working relationships with a broad range of colleaguesDemonstrate ability to work with minimal supervision and within budget and scheduleGood understanding of the clinical trial process, clinical technology and terminologyEnsure data system compliance and in-depth knowledge of 21 CFR Part 11

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Job Source: Ziprecruiter (Will expire by: 2021-01-04 00:00:00)

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