Wendy Tate, PhD, GStat
Product Strategy Director, 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
Q&A Part II with Dr. Wendy Tate, Author of Insights Accrual Prediction Algorithm
This March, Insights Accrual Prediction platform was released to pilot customers. The second issue of our Q&A series continues our conversation with Dr. Wendy Tate, the author behind the machine learning tool’s algorithm, to hear her experience bringing this innovative tool to the research community and get her perspective on what comes next.
Q&A Part I with Dr. Wendy Tate, Author of Insights Accrual Prediction Algorithm
This March, Insights Accrual Prediction platform was released to pilot customers. We sat down with Dr. Wendy Tate, the author behind the machine learning tool’s algorithm, to learn what inspired her to tackle this industry hurdle and hear her experience bringing this innovative tool to the research community.
Clinical Trial Feasibility: Ensuring Success for Clinical Sites
With comprehensive research portfolios and a myriad of operational challenges to manage, it has never been more important for sites to approach research operations as a business.
Key Considerations for Regulatory Compliant Document Storage
It is imperative that your organization has a reliable eRegulatory system and associated policies for storage and upkeep of clinical trial documents to ensure 21 CFR Part 11 compliance. Read our Key Considerations for Regulatory Compliant Document Storage.
Creating an Integrated Approach to Regulatory Management at Your Institution
Over the past year, clinical research professionals have faced unprecedented challenges related to both the clinical and operational management of their research. Maintaining regulatory compliance and visibility within an increasingly remote environment has been a key focus area for many institutions.
Addressing Key COVID-19 Challenges Through Enterprise Technology
November 5, 2020
Throughout the COVID-19 pandemic, research institutions have addressed a wide array of challenges to keep research moving. As we look forward, many institutions still have unanswered questions on how to ...
From Reactive to Proactive: How to Evolve Your Research Program During a Global Crisis
August 5, 2020
Many research programs are evaluating how to keep research moving forward in the face of critical staff shortages and budget limitations—during the COVID-19 pandemic and beyond. Sites are busier than ...
Q&A – The New Normal: Considerations for Restarting Research
Experts answer some of the most popular audience questions from the recent webinar The New Normal: Considerations for Restart Research. Read more:
Study Activation: A Complex Process That Doesn’t Have to Be Painful
If the clinical development time of a new treatment is to ever decrease, reducing the time in study activation is necessary so actual research can be done.
How Research Informs the COVID-19 Response
Research doesn’t just inform medical treatment; it informs public health and public policy, and it helps explain human behaviors. Read more:
Survey Best Practices for Process Improvement
Learn best practices of survey creation to help measure process improvement among stakeholders at an organization.
Beginner’s Guide to Clinical Trial Performance Metrics
Learn what clinical trial performance metrics are, why they are important and which key metrics for clinical trials you should be measuring.