Wendy Tate, PhD, GStat
Director, Advanced Analytics and Research Optimization, Advarra
Wendy Tate’s work is focused on the evaluation of clinical research administration, including the development and testing of quantitative methods to measure and assess protocol feasibility and workload. Her passion is to provide helpful and meaningful processes and tools to clinical research professionals that streamline clinical research practices and better the clinical research enterprise as a whole. Prior to Advarra, Tate spent 15 years at the University of Arizona in various roles within human laboratory, human subjects protection, and clinical research roles, including leadership roles with the IRB and Cancer Center clinical trials office.
Latest Posts by Wendy
Strategies for Successful Site Selection in Clinical Trials
While clinical trial site selection aids in a trial’s success, it’s critical to maximize the study's time, resources, and funds.
Metrics to Increase Macro and Micro Visibility into Site Activity
Explore tools and metrics designed to best measure site performance and engagement on a macro and micro level.
Enhancing Research Conduct Using eConsent
The Belmont Report established informed consent parameters in 1976, but there are no federal regulations surrounding electronic consent.
Trend Forecasting: What Does 2022 Have In Store for Clinical Research?
What will be the 2022 trends in clinical research? In this episode, we forecast what is coming up for clinical trials.
The Clinical Research Training Program Checklist: What to Look For
Most training programs are outdated, unengaging, & redundant. Learn how to make a program achieving both regulatory requirements & your goals
Creating Opportunities for Inclusion, Diversity, Equity and Access In Clinical Research: A Discussion with Tiffany Danielle Pineda, Brian Sevier, and Wendy Tate
December 1, 2021
About the Advarra In Conversations With… The future of healthcare innovation hinges on research and clinical trials. Advarra sits down...
Clinical Research Staffing Reprioritizations and Resourcing Strategies
Gain insights on how to work through staffing reprioritizations and options to consider when planning resourcing strategies.
Wendy Tate and Dylan Rosser Talk Metrics in Clinical Research
In this podcast, we delve into the importance of data collection in clinical research and share tips to leverage metrics.
Study Activation: Top Four Takeaways from Research Sites
How can sponsors leverage their relationship with their sites to ensure more efficient research?
The Current State of Study Activation and Methods to Ensure Success
This webinar will discuss the importance of protocol feasibility and identifying solutions to ensure your organization's success.
Q&A Part II: Clinical Trial Feasibility: Ensuring Success for Clinical Sites
Part 2 of Q&A from the Clinical Trial Feasibility: Ensuring Success for Clinical Sites webinar outlining why it is important for sites to approach research operations as a business.
Q&A Part I: Clinical Trial Feasibility: Ensuring Success for Clinical Sites
Q&A from the Clinical Trial Feasibility: Ensuring Success for Clinical Sites webinar outlining why it is important for sites to approach research operations as a business.