3 Day Virtual Biostatistics for the Non-Statistician Training Course, July 14-16, 2021 - ResearchAndMarkets.com

DUBLIN--()--The "Biostatistics for the Non-Statistician Training Course" conference has been added to ResearchAndMarkets.com's offering.

The focus of the seminar is to give you the information and skills necessary to understand statistical concepts and findings as applies to clinical research and to confidently convey the information to others.

Statistics is a useful decision-making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on the development of a drug or procedure, it is imperative that decision-makers understand the theory and application of statistics.

Many statistical softwares are now available to professionals. However, these softwares were developed for statisticians and can often be daunting to non-statisticians. How do you know if you are pressing the right key, let alone performing the best test?

This seminar provides a non-mathematical introduction to biostatistics and is designed for non-statisticians. And it will benefit professionals who must understand and work with study design and interpretation of findings in a clinical or biotechnology setting.

Emphasis will be placed on the actual statistical (a) concepts, (b) application, and (c) interpretation, and not on mathematical formulas or actual data analysis. A basic understanding of statistics is desired, but not necessary.

Seminar Includes: Certificate, PDF copy of the Handouts, Q/A Session, Live Instructor-led 3 Days Web Seminar & Statistical Analysis Plan Template provided by the faculty.

Learning objectives

  • The goal of this seminar is to teach you enough statistics to:
  • Understand the statistical portions of most articles in medical journals.
  • Do simple calculations, especially ones that help in interpreting published literature.
  • Avoid being misled by foolish findings.
  • Knowledge of which test when, why, and how.
  • Perform simple analyses in statistical software.
  • Communicate statistical findings to others more clearly.

Who Should Attend:

  • Physicians
  • Clinical Research Associates
  • Clinical Project Managers/Leaders
  • Sponsors
  • Regulatory Professionals who use statistical concepts/terminology in reporting
  • Medical Writers who need to interpret statistical reports
  • Clinical research organizations, hospitals, researchers in health and biotech fields.
  • Persons working in the medical or health sciences, pharmaceutical and or nutriceutical industries, clinical trials, clinical research, and clinical research organizations, physicians, medical students, graduate students in the biological sciences, researchers, and medical writers who need to interpret statistical reports.


Day 1: Basics

Session 1: Why Statistics

  • Do we really need statistical tests?
  • Sample vs. Population
  • I'm a statistician, not a magician! What statistics can and can't do
  • Descriptive statistics and measures of variability

Session 2: The many ways of interpretation

  • Confidence intervals
  • p-values
  • Effect sizes
  • Clinical vs. meaningful significance

Session 3: Types of Data and Descriptive Statistics

  • Levels of data: Continuous, Ordinal, Nominal
  • Normal distribution and its importance
  • Graphical representations of data
  • Data transformations, when and how

Session 4: Common Statistical Tests

  • Comparative tests
  • Simple and Multiple regression analysis
  • Non-parametric techniques


Day 2: Further Understanding in Clinical Research

Session 1: Other Tests

  • Non-Parametric tests
  • Test for equivalency
  • Test for non-inferiority

Session 2: Power and Sample Size

  • Theory, steps, and formulas for determining sample sizes
  • Demonstration of sample size calculations with GPower software

Session 3: How to Review a Journal Article

  • General steps on article review
  • Determining the quality of a journal or journal article
  • Looking for limitations (all studies have them)
  • Review of a selection of journal articles for quality and interpretation

Session 4: Developing a Statistical Analysis Plan

  • Using FDA (for the U.S. audience) or MHRA (for U.K. audience) guidance as a foundation, learn the steps and criteria needed to develop a statistical analysis plan (SAP)
  • An SAP template will be given to all attendees

Day 3: Special Topics

Session 1: Logistic Regression

  • When and why?
  • Interpretation of odd ratios
  • Presentation of logistic regression analysis and interpretation
  • Fun with contingency tables

Session 2: Survival Curves and Cox Regression

  • History, theory, and nomenclature of survival analysis
  • Kaplan-Meier Curves and Log Rank Tests
  • Proportional Hazards
  • Interpretation of hazard ratios
  • Presentation of KM curves and Cox regression analysis and interpretation

Session 3: Bayesian Logics

  • A different way of thinking
  • Bayesian methods and statistical significance
  • Bayesian applications to diagnostics testing
  • Bayesian applications to genetics

Session 4: Systematic Reviews and Meta-Analysis

  • Why perform a systematic review and/or meta-analysis?
  • A bit of history and reasoning for systematic reviews and/or meta-analysis
  • Terminology
  • Steps in performing a Systematic Review
  • Steps in performing a Meta-Analysis

For more information about this conference visit https://www.researchandmarkets.com/r/j9wgka


Laura Wood, Senior Press Manager
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900


Laura Wood, Senior Press Manager
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900