In this online course, you will learn basics and advanced SAS clinical programming concepts to read and manipulate clinical data. Using the clinical features and basic SAS programming concepts of clinical trials, this course shows how to import ADAM, CDISC or other standards for domain structure and contents into the metadata, build clinical domain target table metadata from those standards, create jobs to load clinical domains, to validate the structure and content of the clinical domains based on the standards, and to generate CDISC standard define.xml files describing the domain tables for clinical submissions. Training type: OnlineDuration: 4-5 WeeksBatch Timings: Morning, Evening and Weekend batches available Who should attend? Bioinformatics or Life Science Graduates Job aspirants with basic understanding of clinical programming concepts or statistics Clinical SAS Programming is used for Clinical Data Integration, Organizing, Standardizing and Managing clinical research data and metadata. It provides the foundation you need to ensure standard, trusted clinical data to support strategic analyses, such as cross-study and advanced safety analysis. With SAS Clinical Programming, you can gain both speed and efficiency by automating repeatable clinical data integration tasks. Class size is limited—sign up for this course today! Course Highlights(Below outlines are only a small part of the full curriculum) BASE SAS and Advance SAS: Basic SAS Concepts Referencing files, setting Options, Editing and debugging SAS Programs Creating List Reports and Enhanced List and summary reports Creating SAS data sets from raw data Understanding DATA step processing Creating and applying user defined formats Producing descriptive Statistics Creating and managing variables Reading SAS Data sets Combining SAS data sets Transferring Data with SAS functions Generating Data with DO loops and processing variables with Array Reading Raw Data in fixed fields Advanced Base/SAS: Macros and Proc Sql Advanced Base/SAS: Certification Steps SAS Clinical Programming Explanation of organizational aspects of the Biometrics department Basic concepts of Clinical trials Phase – I, Phase – II, Phase – III, Phase – IV Data Management&Statistical Methods in Clinical Trails Access DICTIONARY Tables using the SQL procedure Explanation of the Clinical trial process Protocol development CRF Design and development, Data Management plan Principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices Edit check specifications document, Edit check programming Data querying, Paper CRF and E-CRF studies Database programming and basic understanding of EDC studies Annotated CRF’s Data Querying Lab data handling – procedures and pitfalls Patient Profiles, Database Lock MedDRA®: Overview CDISC (ODM, SDTM, ADaM and Define.XML), SDTM 3.1.2 and ADAM 1.2 Implementation Clinical SAS Certification Steps Resume Formatting Mock Interviews by SAS Clinical Programmers Job Placement Marketing For full curriculum and details contact training@serigor.com or call us at +1-443-687-9600
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