ArchiTech IT

Course information

We provide the best SAS Clinical /Clinical SAS training with the Clinical knowledge which always have an competitive edge over a purely SAS programmer as he/she will be in a position to take decisions while programming whose primary responsibility is writing programs in SAS to generate the output (tables, listings, and figures) needed for the analysis and reporting of the clinical study. A familiarity with Clinical SAS Programmer having CDISC (standard specifications for electronically submitted clinical data) expertise would have extensive opportunities.

Domain
Clinical research Process
Data management Advanced
Study Protocol Briefing and Extraction
CRF design
Database spec and Edit check preparation
OC/RDC
Administration
PL/SQL basics
Users, Roles, Assigning user roles, User specific screens management
PSUB, batch jobs administration
Glib Admin – Reference codelists
Study Plan
Design – Create and maintain – Studies, Investigators, Sites,Visits and patients
Definitions
DVGs
Questions, Question Groups
DCM
DCI
Validation programming
Data extract views administration
Test a study
Test Data entry
Conduct
Data validation (Discrepancy management)
Execute – Batch jobs, Procedures, DCF forms.
Data Extract
Batch data, Out of study data load
Conduct security
Patient lock and freeze, study lock and freeze
Mass changes
Data entry (first pass, second pass), update, browse and key changes.
Lab data load and administration
RDC Administration
RDC Workflow and discrepancy management
TMS
Integration OC AE term, MT term and conmed terms with TMS and medical coding and review
TMS dictionary and maintenance