Hello, I am Deependra from IDC. I have a C2C position name is "SAS Programmer". Please revert back to me if you are interested.
Role: Sr. SAS Programmer Location: North Chicago, IL (Remote till covid) Rate: $58/HR on C2C Exp.: 8+ years Job Description: * 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 SDTM, ADaM datasets. * Map raw data to SDTM (Study data table model) in compliance with CDISC data model standards and create specifications for programming. * 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: * Bachelor's degree in Computer Science, Statistics, Engineering or related field with minimum 6 years of related experience. * Required skills: create SDTM datasets from raw data according to CDISC standards; 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). Thanks and Regard; Deependra Kumar IDC Technologies Inc. Location: Pleasanton, CA Email: [email protected]<mailto:[email protected]> Phone: (321)-465-8215 Website: idctechnologies.com<http://idctechnologies.com/> -- You received this message because you are subscribed to "rtc-linux". Membership options at http://groups.google.com/group/rtc-linux . Please read http://groups.google.com/group/rtc-linux/web/checklist before submitting a driver. --- You received this message because you are subscribed to the Google Groups "rtc-linux" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To view this discussion on the web visit https://groups.google.com/d/msgid/rtc-linux/DX1P273MB0505EAE07B69623B81ECE209F66A9%40DX1P273MB0505.AREP273.PROD.OUTLOOK.COM.
