Debi O

Debi Smith is a highly skilled and experienced clinical research professional with a diverse background in regulatory affairs, clinical research, and safety management. She holds a Bachelor's degree in Mathematics-Economics and French from Agnes Scott College and a regulatory affairs certificate in Pharmaceuticals and Medical Devices from the Regulatory Affairs Professional Society (RAPS). With years of experience in the industry, Debi has held various senior positions at Covance, Sarah Cannon Research Institute, Kentucky Medical Research Center, and Sterling IRB.

Debi's expertise lies in the management of regulatory and clinical affairs activities for pharmaceutical and medical device industries. She has held various positions throughout her career, including Sr. Clinical Research Associate, Manager of Regulatory Operations, Senior Regulatory Affairs Specialist, and more. Her experience makes her a valuable asset to any organization looking to navigate the complex regulatory landscape of clinical research today.