Hi
Hope you are doing good. We are looking for Clinical SAS Programmer in Plymouth Meeting, PA. If you would be interested please share updated resume at [email protected]<mailto:[email protected]> Location - Plymouth Meeting, PA 19462 Job Description Clinical SAS Programmer Summary: Responsible for loading, documenting, and cleaning large and complex health care data sets, creating analytical data files, and running statistical analyses sources while following the clinical study's protocol or statistical plans. Available to help investigators, junior researchers, and other staff with the use of data files within various clinical research projects. Perform technical research, system integration, daily support, risk analysis, supportability and effectiveness analyses for assigned task. Primary Responsibilities: * Documents and archives all aspects of analyses and data management. * Other responsibilities as assigned by the supervisor. * Build SAS datasets from clinical database. * Develop SAS macros, templates and utilities for data cleaning and reporting. * Utilize SDTM guidelines to build datasets. * Communicate with an internal team to create deliverables for pharmaceutical and biotechnology clients. * Implement analyses specified in the protocol or the Statistical Analysis Plan (SAP) while working with the project statistician. * Ensure CRF meets the guidelines of the protocol and check for consistency and adequacy. * Write SAS programs to generate tables, listings, and figures and analysis datasets. * Review CRF annotations and data specifications. * Work in tandem with Biostatistics and Data Management member on various clinical projects. * Identify and edit checks per the data validation plan or data management plan. * Study management reports using SAS. * Validate the programmed analysis datasets, tables, listing and figures. * Perform analyses defined in the statistical analysis. * Prepare clinical and statistical summary reports. * Communicate with programming and statistics leads. * Utilize SAS programming skills within protocol team and perform all programming required for clinical trial analysis and reporting. * Perform quality control on final reports. * Develop SAS coding and table templates for preparing, processing and analyzing clinical data. * Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues. * Provide On-Call support. * Manage Team Clinical SAS Programmer Additional Responsibilities * To work with Technical Architecture, Project Management, Application Services and client representatives to validate Technical Architecture designs and to build/implement solutions. * Completes implementation tasks, with attention to detail and while under pressure. * Responsible for ensuring compliance and update to the documentation framework to support Data Management. * Responsible for loading, validating, documenting, managing, and analyzing data for both internal and collaborative research projects. * Responsible for assisting with data storage and management issues around both new and ongoing projects within the Division. * Responsible for working with other research staff within the Division to help specify appropriate analytical data files for the research question under investigation. * Responsible for creating and carefully documenting all derived analytical data files so that they can be understood and used by other members of the research team. * Accurately produce low level design documentation. Knowledge, Skills and Abilities * Base SAS * ACCESS Interface to ODBC * MS SQL Server * SAS Studio * SAS Clinical Standard Toolkit knowledge CDISC standards like STDM, CRT-DDS, Define-XML 2.0, Define-XM, ADaM 2.1, CDASH 1.1, SEND 3.0. * ability to manage and prioritize multiple projects (Studies). * ability to work effectively as a member of a multidisciplinary research team * Knowledge in ticketing process in Jira & Service Now, Confluence. Complexity Work on issues of diverse scope where analysis of situation or data requires evaluation of a variety of factors, including an understanding of current Data Transfer Plan needs. Interaction Frequently interacts with subordinate supervisors. Supervision Manages, perhaps through subordinate supervisors, the coordination of the activities of a section with responsibility for results. Education Minimum Bachelors/Master's preferred. Professional certification related to area of assignment may be required Experience 5+ years of experience with SAS programming in a health care environment. Proficiency with SAS/BASE (Data step programming) and SAS/SQL or other relational database software (e.g., MS SQL Server), experience working with health care data. Regards, [cid:[email protected]] Bhavnish Wadhwa | Executive - RMG 485 Alberto Way, Los Gatos, CA 95032 O: +1 408-872-4106 M: +1 408-389-1425 infogain.com<http://www.infogain.com/> | Engineering Business Outcomes -- 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]. 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