2-Day Seminar Completed | Recording and Pre-Registration Available


Seminar Registration Options: *

Learn More


If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you.

Pre-Register now and pay only once the training is scheduled on your preferred days.

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 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.


The goal of this seminar is to teach you enough statistics to:

  1. Understand the statistical portions of most articles in medical journals.
  2. Do simple calculations, especially ones that help in interpreting published literature.
  3. Avoid being misled by foolish findings.
  4. Knowledge of which test when, why, and how.
  5. Perform simple analyses in statistical software.
  6. Communicate statistical findings to others more clearly.

  • Physicians
  • Clinical Research Associates
  • Clinical Project Managers/Leaders
  • Sponsors
  • Regulatory Professionals who use statistical concepts/terminology in reporting
  • Everyone working in the medical or health sciences, pharmaceutical and or nutraceutical 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 (11 AM to 5 PM)

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: Common Statistical Tests
• Comparative tests
• Regression analysis
• Non-parametric techniques

Session 4: Bayesian Logic
• A different way of thinking
• Bayesian methods and statistical significance
• Bayesian applications to diagnostics testing
• Bayesian applications to genetics

DAY 2 (11 AM to 5 PM)

Session 1: Systematic Reviews and Meta-Analysis
• Why perform a systematic reviews 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

Session 2: Study power and sample size
• Review of p-value, significance level, effect size
• Formulas, software, and other resources for computing a sample size

Session 3: Developing a Statistical Analysis Plan
• Using FDA 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.

Session 4: Specialized topics & Other Tests
• Survival Curves and Cox Regression
• Logistic Regression
• Taking a holistic view to study design and interpretation
• Non-Parametric tests
• Test for equivalency
• Test for non-inferiority
• Question and Answer session


Elaine Eisenbeisz is a private practice statistician and owner of Omega Statistics, a statistical consulting firm based in Southern California. Elaine has over 30 years of experience in creating data and information solutions for industries ranging from governmental agencies and corporations, to start-up companies and individual researchers.

Elaine’s love of numbers began in elementary school where she placed in regional and statewide mathematics competitions. She attended University of California, Riverside, as a National Science Foundation scholar, where she earned a B.S. in Statistics with a minor in Quantitative Management, Accounting. Elaine received her Master’s Certification in Applied Statistcs from Texas A&M, and is currently finishing her graduate studies at Rochester Institute of Technology. Elaine is a member in good standing with the American Statistical Association as well as many other professional organizations. She is also a member of the Mensa High IQ Society. Omega Statistics holds an A+ rating with the Better Business Bureau.

Elaine has designed the methodology for numerous studies in the clinical, biotech, and health care fields. She currently is an investigator on approximately 10 proton therapy clinical trials for Proton Collaborative Group, based in Illinois. She also designs and analyzes studies as a contract statistician for nutriceutical and fitness studies with QPS, a CRO based in Delaware. Elaine has also worked as a contract statistician with numerous private researchers and biotech start-ups as well as with larger companies such as Allergan and Rio Tinto Minerals. Not only is Elaine well versed in statistical methodology and analysis, she works well with project teams. Throughout her tenure as a private practice statistician, she has published work with researchers and colleagues in peer-reviewed journals. Please visit the Omega Statistics website at www.OmegaStatistics.com to learn more about Elaine and Omega Statistics.