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Cheryl Byers, MHA, CIP, CHRC

VP & Principal, Advarra Consulting Institutional Research CoE, Advarra

With over 20 years’ research compliance experience, Cheryl Byers is an expert in human subject research. She has provided oversight to programs such as pre-clinical, conflict of interest, HIPAA Privacy, research misconduct, institutional biosafety, radiation safety, export control, and facility security. Byers is a former AAHRPP site visitor and step 1 reviewer; is certified in healthcare research compliance; and is a certified IRB professional.

Cheryl Byers

Latest Posts by Cheryl

 
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

Phase I Oncology Clinical Trials

This blog discusses what makes Phase I oncology trials complex and what IRBs need to know as they review a Phase I trial.

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4 min. read
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Podcast

Cheryl Byers and Dr. John H. Stewart Discuss Diversity, Equity and Inclusion in Cancer Research

Diversity, equity, and inclusion (DEI) in cancer research are critical to clinical research. In this episode, Advarra’s Cheryl Byers and Dr. John H. Stewart have a discussion on what is DEI, the current climate of DEI in cancer research, and considerations to improve DEI in clinical trial enrollment and retention.

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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

Legislation to Advance Equality and Inclusion in Oncology Clinical Trials

The Clinical Treatment Act and Henrietta Lacks Enhancing Cancer Research Act aims to increase diversity in oncology clinical trials

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4 min. read
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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

Community-Based Participatory Research (CBPR): A Framework for Community Engagement

Community-based participatory research (CBPR) is utilized to reduce racial and ethnic health disparities in under-represented populations.

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4 min. read
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