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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

 
Webinar

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.

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Webinar

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 ...

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Webinar

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 ...

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Blog

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:

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7 min. read
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Webinar

The New Normal: Considerations for Restarting Research

June 3, 2020

Throughout the COVID-19 pandemic, we have continually heard what the “new normal” could mean for our work lives, social lives, schools, communities, and our medical system. But what does it ...

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Blog

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.

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3 min. read
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Blog

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:

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5 min. read
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Blog

Survey Best Practices for Process Improvement

Learn best practices of survey creation to help measure process improvement among stakeholders at an organization.

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5 min. read
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