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Biostatistics in R: Clinical Trial Applications

taught by Din Chen
and Karl Peace


Brief Description:

This course covers the implementation in R of statistical procedures important for the clinical trial statistician.

Instructor(s):
Level: Intermediate / Introductory

Who Should Take This Course:

Analysts and statisticians at pharmaceutical companies and other health research organizations who need or want to become involved in the design, monitoring or analysis of clinical trials and who are familiar with R software and considering its use in clinical trials.

Dates:
May 25, 2012 to June 22, 2012November 16, 2012 to December 14, 2012
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Biostatistics in R: Clinical Trial Applications

taught by Din Chen
and Karl Peace

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Registration:
Please read the syllabus tab, noting the prerequisites, text and software requirements.

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Biostatistics in R: Clinical Trial Applications

taught by Din Chen
and Karl Peace



Aim of Course:

This course covers the implementation in R of statistical procedures important for the clinical trial statistician.  Students completing the course will learn how to use R to compare treatments, incorporate covariates into the analysis, analyze survival (time-to-event) trials, model longitudinal data, and analysis of bioequivalence trials.

This course is a core requirement or elective in the following Program(s) in Analytics and Statistical Studies (PASS):

Prerequisite(s):

Course Program:

SESSION 1: Treatment Comparisons

  • R fundamentals associated with clinical trials
  • A simple simulated clinical trial
  • Statistical models for treatment comparisons
  • Incorporating covariates

SESSION 2: Survival Analysis

  • Time-to-event data structure
  • Statistical models for survival data
  • Right-censored data analysis
  • Interval-censored data analysis

SESSION 3: Analysis of Data from Longitudinal Clinical Trials

  • Trial designs and data structure
  • Statistical models and analysis

SESSION 4: Analysis of Bioequivalence Clinical Trials

  • Data from bioequivalence clinical trials
  • Bioequivalence clinical trial endpoints
  • Statistical methods to analyze bioequivalence

HOMEWORK:

Homework in this course consists of short answer questions to test concepts, guided data analysis problems using software, and guided data modeling problems using software.

Organization of the Course:

This course takes place over the internet at the Institute for 4 weeks. During each course week, you participate at times of your own choosing - there are no set times when you must be online. Course participants will be given access to a private discussion board. In class discussions led by the instructor, you can post questions, seek clarification, and interact with your fellow students and the instructor.

The course typically requires 15 hours per week. At the beginning of each week, you receive the relevant material, in addition to answers to exercises from the previous session. During the week, you are expected to go over the course materials, work through exercises, and submit answers. Discussion among participants is encouraged. The instructor will provide answers and comments, and at the end of the week, you will receive individual feedback on your homework answers.


Credit:
Students come to the Institute for a variety of reasons. As you begin the course, you will be asked to specify your category:
  1. You may be interested only in learning the material presented, and not be concerned with grades or a record of completion.
  2. You may be enrolled in PASS (Programs in Analytics and Statistical Studies) that requires demonstration of proficiency in the subject, in which case your work will be assessed for a grade.
  3. You may require a "Record of Course Completion," along with professional development credit in the form of Continuing Education Units (CEU's).  For those successfully completing the course, 5.0 CEU's and a record of course completion will be issued by The Institute, upon request.

Course Text:

The course text is Clinical Trial Data Analysis Using R by Ding-Geng (Din) Chen and Karl E. Peace, which you can order from CRC Press, or by using this form. CRC Press typically gives students a generous discount when students order the text using the above form (not by ordering the text online).

PLEASE ORDER YOUR COPY IN TIME FOR THE COURSE STARTING DATE.


Software:

You must have a copy of R for the course. Click Here for information on obtaining a free copy.

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Biostatistics in R: Clinical Trial Applications

taught by Din Chen
and Karl Peace



Instructor(s):
Dates:
May 25, 2012 to June 22, 2012November 16, 2012 to December 14, 2012
Course Fee: $499
Academic Rate: $399

Before registering, please read the syllabus tab, noting the prerequisites, text and software requirements. When you click the register button, you will be taken to our secure transaction page.

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