| Need SAS Data Programmer - North Chicago, IL - ONSITE - Contract at Chicago, Illinois, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=212797&uid= From: Vinod, Themesoft Inc [email protected] Reply to: [email protected] Good Afternoon, Hope you are doing well. My name is Vinod from Themesoft. Please find the job description below. Kindly send me your / consultant updated resume to proceed further. Job Details: Title: SAS Data Programmer Location: North Chicago, IL - ONSITE Duration: 6 months + Contract Major Tasks of Position: 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 datasets. Create ADaM Specifications & datasets from SDTM datasets per CDISC analysis data model standards and SAP. Provide validation support to create SDTM+, SDTM and/or ADaM datasets / 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 SDTM, ADaM datasets, statistical tables, listings, and graphs Requirements: Demonstrate proficiency of programming skills. Must have exp of ONC and 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. QC experience. Work Interactions: Early Clinical Leaders / Global Clinical Leaders Global Safety Leaders/ Data managers Statisticians and Statistical Analysts Qualifications: Bachelors degree in Computer Science, Statistics, mathematics, Engineering or related field with minimum 6 years of related experience. Preferrable degree with Statistics or mathematics cources Required skills: Create ADAM datasets from SDTM datasets according to 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) Thank you Vinod Keywords: active directory http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=212797&uid= |
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| 03:37 PM 15-Dec-22 |