
Cheryl Byers, MHA, CIP, CHRC
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

Navigating sIRB Complexities: An Interactive Session
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and...
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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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Clinical Trial Feasibility: Ensuring Success for Clinical Sites
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and...
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Phase I Oncology Clinical Trials
In a recent blog, we described the complexity and uniqueness of Phase I clinical trials,...
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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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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...
Read More...