Cheryl Byers, MHA, CIP, CHRC

VP & Principal, 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.

Latest Posts by Cheryl Byers

E-Book

Setting Yourself up for Success During Investigator-initiated Trials

This eBook outlines Tips and best practices for a successful IIT, Post-approval monitoring and clinical...

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E-Book

Phase I Oncology Clinical Trials

In a recent blog, we described the complexity and uniqueness of Phase I clinical trials,...

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E-Book

Q&A Part II: Clinical Trial Feasibility: Ensuring Success for Clinical Sites

In a recent webinar, Advarra experts Wendy Tate and Cheryl Byers provided considerations for building...

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E-Book

Q&A Part I: Clinical Trial Feasibility: Ensuring Success for Clinical Sites

In a recent webinar, Advarra experts Wendy Tate and Cheryl Byers provided considerations for building...

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E-Book

Legislation to Advance Equality and Inclusion in Oncology Clinical Trials

According to the Association for Clinical Oncology, individuals who identify as African American or Black...

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E-Book

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

Community-based participatory research (CBPR) continues to come up in conversations surrounding diversity and inclusion in...

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