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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.

Wendy Tate

Latest Posts by Wendy

 
Podcast

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...

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Webinar

Clinical Research Staffing Reprioritizations and Resourcing Strategies

Gain insights on how to work through staffing reprioritizations and options to consider when planning resourcing strategies.

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Podcast

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.

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Blog

Study Activation: Top Four Takeaways from Research Sites

How can sponsors leverage their relationship with their sites to ensure more efficient research?

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5 min. read
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Webinar

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.

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Blog

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.

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5 min. read
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Blog

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.

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4 min. read
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Blog

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.

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5 min. read
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Blog

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.

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6 min. read
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White Paper

Case Studies in Accrual Prediction

Accrual is the ultimate outcome of success for a clinical trial. Reports estimate that at the site-level 30%-50% of studies close with zero-accrual.

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Webinar

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.

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Blog

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.

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5 min. read
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