SAS Clinical Training and Placement Program by Showtheropes

For full curriculum and batch details contact training@serigor.com or call us at +1-443-687-9600 Visit us at http://www.showtheropes.com Course Details: In this course, you will learn basics and advanced SAS concepts to read and manipulate clinical data. Using the clinical features and basic 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: Online Duration: 4-5 Weeks Batch Timings: Morning, Evening and Weekend batches available Who should attend? Bioinformatics or Life Science Graduates Job aspirants with basic understanding of clinical concepts or statistics SAS Clinical Data Integration organizes, standardizes and manages 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, you can gain both speed and efficiency by automating repeatable clinical data integration tasks. Class size is limited?sign up for this course today! What you?ll learn? 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 Clinical Programming Explanation of organizational aspects of the Biometrics department Basic concepts of Clinical trials Phase ? I, Phase ? II, Phase ? III, Phase ? IV Clinical trial glossary ? Demystified Explanation of the Clinical trial process Protocol development CRF Design and development, Data Management plan 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 CDISC SDTM 3.1.2 and ADAM 1.2 Implementation How to generate Tables, Listing and Figures For full curriculum and batch details contact training@serigor.com or call us at +1-443-687-9600 Visit us at http://www.showtheropes.com Weniger lesen