Clinical Online Training
Clinical Online Training at Learn SAS Online Institute in Hyderabad is an innovative and interactive way to learn SAS programming. The course is designed for those who wish to pursue a career in the pharmaceutical and/or clinical research industry. The course covers all the basics of SAS programming, including data entry, cleaning, manipulation, and analysis. In addition, the course provides an overview of the different types of clinical trials, their design, and execution. The course is taught by experienced faculty who have worked in the industry for many years.
Are you looking to advance your career in the healthcare industry but finding it difficult to attend traditional classroom-based training programs? Look no further! Learn SAS Online Institute in Hyderabad offers comprehensive clinical online training courses that can help you gain the necessary skills and knowledge from the comfort of your own home. Whether you are a medical professional, researcher, or student, our expert instructors will guide you through real-world scenarios and hands-on exercises using state-of-the-art technology. Join us now to take advantage of this exciting opportunity and take your career to new heights!
Why to do this course?
In the drug development industry, SAS plays an important and essential role in the research and development of drugs, diagnostics, and medical devices. Familiarity with Clinical Online Training programming skills can lead to a challenging and rewarding career that also positively impacts and transforms patients’ lives.
Learn SAS Online is the best online training institute in Hyderabad to offer Clinical Online Training well-focused and career-oriented training program in Clinical SAS.
What are the prerequisites for this course?
The prerequisites for this Clinical online training are a basic understanding of medical terminology, anatomy, and physiology. In addition, students should have basic computer skills and be comfortable using the Internet.
Benefits of Learning Clinical SAS
Learn SAS Online Institute in Hyderabad offers clinical online training that helps you become a certified SAS programmer. This certification will help you get a job in the healthcare industry, where SAS programming is in high demand. The institute’s online training program is designed to give you the skills and knowledge you need to succeed in your career.
Include:
- You will learn from experienced SAS instructors who are experts in the field.
- The institute's online training program is comprehensive and covers all aspects of clinical SAS programming.
- You can study at your own pace and complete the course within a few weeks.
- The institute offers flexible payment options, so you can pay for the course as you go.
- You will receive a certificate of completion upon successful completion of the course.
Course Structure
- Clinical Trials Process
- Clinical Trials Data Structures
- Import and Export Clinical Trials Data
- Manage Clinical Trials Data
- Transform Clinical Trials Data
- Apply Statistical Procedures for Clinical Trials
- Macro Programming for Clinical Trials
- Report Clinical Trials Results
- Validate Clinical Trial Data Reporting
Advantages of Taking a Clinical Online Training Course
- Flexibility and Convenience
- Diverse Range of Topics
- Interactive Learning Materials
- Expert Instruction
- Certification and Continuing Education
- Networking Opportunities
- Access to the Latest Research and Updates
- Cost-Effectiveness
SAS is the de facto industry standard for clinical data analysis and reporting in the life sciences/pharmaceutical industry. This course will give the capability for the candidate how to apply SAS programming skills to clinical trials data.
Duration: 15-20 hours
Course Content
Describe the clinical research process (phases, key roles, key organizations).
Interpret a Statistical Analysis Plan.
Derive programming requirements from an SAP and an annotated Case Report Form.
Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices).
Identify the classes of clinical trials data (demographic, lab, baseline, concomitant medication, etc.).
Identify key CDISC principals and terms.
Describe the structure and purpose of the CDISC SDTM data model.
Describe the structure and purpose of the CDISC ADaM data model.
Describe the contents and purpose of define.xml.
Apply regulatory requirements to exported SAS data sets (SAS V5 requirements).
Access DICTIONARY Tables using the SQL procedure.
Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc).
Apply categorization and windowing techniques to clinical trials data.
Transpose SAS data sets.
Apply ‘observation carry forward’ techniques to clinical trials data (LOCF, BOCF, WOCF).
Calculate ‘change from baseline’ results.
Obtain counts of events in clinical trials.
Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, SUMMARY).
Use PROC FREQ to obtain p-values for categorical data (2×2 and NxP test for association).
Use PROC TTEST to obtain p-values for continuous data (one-sample, paired and two-sample t-tests).
Create output data sets from statistical procedures.
Create and use user-defined and automatic macro variables.
Automate programs by defining and calling macros.
Use system options to debug macros and display values of macro variables in the SAS log (MPRINT, SYMBOLGEN, MLOGIC, MACROGEN).
Use PROC REPORT to produce tables and listings for clinical trials reports.
Use ODS and global statements to produce and augment clinical trials reports.
Explain the principles of programming validation in the clinical trial industry.
Utilize the log file to validate clinical trial data reporting.
Use programming techniques to validate clinical trial data reporting (PROC COMPARE, MSGLEVEL).
Identify and Resolve data, syntax and logic errors.