Duration of Hours
Duration time may vary depends on course progress
provides the foundation you need to ensure standard, trusted clinical data to support strategic analyses, such as cross-study and advanced safety analysis SAS is widely used in clinical trial data analysis in pharmaceutical, biotech and clinical research companies. The SAS Global Certification program includes credentials that validate SAS skills in Programming, Analytics, Data Science, Administration, Data Management and Enterprise Business Intelligence.
Training Objectives of SAS CLINICAL:
Clinical trials methodologies
Performing statistical analysis and macro programming
Creating clinical trials graphs
Clinical research Process
Data management Advanced
Study Protocol Briefing and Extraction
Database spec and Edit check preparation
Users, Roles, Assigning user roles, User specific screens management
PSUB, batch jobs administration
Glib Admin – Reference code lists
Design – Create and maintain – Studies, Investigators, Sites, Visits and patients
Questions, Question Groups
Data extract views administration
Test a study
Test Data entry
Data validation (Discrepancy management)
Execute – Batch jobs, Procedures, DCF forms.
Batch data, Out of study data load
Patient lock and freeze, study lock and freeze
Data entry (first pass, second pass), update, browse and key changes.
Lab data load and administration
RDC Workflow and discrepancy management
Integration OC AE term, MT term and combed terms with TMS and medical coding and review
TMS dictionary and maintenance
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Why with us?
Live Quality Training
Live demonstration of of features and practicals.
100% Assurance Placement Assistance
Effective Resume building
Internship Program for real exposure
Interview preparation with mock interview drills
Process of applying jobs at right places
Guidance of getting flexible, part time jobs