top of page

DEDICATED TO PROTECTION THROUGH DATA

The CWD Research Initiative is a clinical organization dedicated to the advancement of scientific knowledge and the protection of public health. We advocate for the CWD Equal Protection Act, ensuring that research findings are translated into actionable legislative policies that safeguard communities and preserve the integrity of our research environment.

Our Research Leaders

Dr. Elena Vance

Lead Research Scientist

Dr. Marcus Thorne

Senior Epidemiologist

Sarah Jenkins

Advocacy Director

Dr. Julian Reed

Senior Researcher

Dr. Naomi Chen

Lead Research Scientist

Robert Vance

Advocacy Director

bottom of page