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Mastering Clinical Data Management and Analysis with SAS
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Mastering Clinical Data Management and Analysis with SAS
Published 2/2024
Created by Uplatz Training
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch
Genre: eLearning | Language: English | Duration: 52 Lectures ( 45h 3m ) | Size: 21.7 GB



Unlock Power of Clinical SAS: From Data Management to Advanced Analysis Techniques for Clinical Research Professionals.




[b]What you'll learn
:
[/b]
Gain a strong foundation in SAS programming principles and techniques
Learn how to manage and manipulate clinical trial data using SAS
Understand CDISC standards and their application in clinical data analysis
Develop skills in creating reports and visualizations for clinical research
Prepare for a career in clinical research using SAS

Requirements:
Enthusiasm and determination to make your mark on the world!

Description:
A warm welcome to the Mastering Clinical Data Management and Analysis with SAS course by Uplatz.Clinical SASis a software suite developed by SAS Institute, a leading provider of analytics and business intelligence solutions. SAS Clinical is specifically designed to support the needs of clinical research organizations and pharmaceutical companies in managing, analysing, and reporting clinical trial data.Some key features of Clinical SASinclude:Data Management: SAS Clinical enables users to efficiently manage and integrate clinical trial data from multiple sources, including electronic health records, case report forms, laboratory data, and patient diaries.Statistical Analysis: The software provides a comprehensive set of statistical tools for analysing clinical trial data, including descriptive statistics, hypothesis testing, regression analysis, survival analysis, and more.Reporting and Visualization: SAS Clinical offers powerful reporting and visualization capabilities, allowing users to create customized reports, tables, graphs, and dashboards to communicate findings and insights effectively.Regulatory Compliance: SAS Clinical is designed to meet regulatory requirements and standards such as FDA's 21 CFR Part 11, ensuring data integrity, security, and compliance with industry regulations.Integration with Other Systems: SAS Clinical can be integrated with other systems and platforms commonly used in clinical research, such as electronic data capture (EDC) systems, clinical trial management systems (CTMS), and data warehouses.SAS Clinical provides a robust and flexible platform for managing and analysing clinical trial data, helping researchers and organizations streamline the drug development process, make informed decisions, and accelerate time to market for new therapies.

Who this course is for:
Data Analysts
Data & Analytics Consultants
Beginners & newbies aspiring for a career in statistics, data analytics, and data science
Anyone interested in SAS - data analytics and clinical research
Clinical SAS Programmers
SAS Clinical Researchers
Pharma & Clinical Business Consultants
Data Scientists & Machine Learning Engineers
Statistical Programmers
Data Management & Governance Experts
Managers - Statistical Programming
Clinical Data Managers
Clinical Database Programmers
Biometricians
Clinical Research Associates (CRA)
Medical Writers
Regulatory Affairs Specialists


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