Katie Keene
About Katie Keene
Katie Keene is a Clinical Research Coordinator with over a decade of experience in the industry, currently working at Nutrasource in Ontario, Canada. She holds a Bachelor of Science degree and is a Certified Clinical Research Professional, specializing in the management of clinical trials and regulatory affairs.
Work at Nutrasource
Katie Keene has been employed at Nutrasource since 2016, currently holding the position of Clinical Research Coordinator. In this role, she manages Investigational Product (IP) receiving, management, and dispensing. Her responsibilities include assisting with Trial Master File set-up, maintenance, and archival at the Contract Research Organization (CRO). Prior to her current role, she worked as a Clinical Trial Project Assistant from 2015 to 2016 and as a Research Assistant from 2012 to 2015. Her extensive experience at Nutrasource contributes to her expertise in clinical trials.
Education and Expertise
Katie Keene holds an Honours Bachelor of Science (BSc) degree in Nutritional and Nutraceutical Sciences from the University of Guelph, which she completed from 2007 to 2011. She also achieved her High School Diploma at O'Neill Collegiate C.V.I. from 2003 to 2007. Additionally, she is a Certified Clinical Research Professional (CCRP), which underscores her commitment to professional development in the clinical research field.
Background
Katie Keene has over a decade of industry experience, primarily in the clinical research and Natural Health Products (NHP) sectors. She has spent more than three years in regulatory affairs and has dedicated over eight years to conducting phase I - IV studies. Prior to her career in clinical research, she worked as a Sales Associate at GNC in Guelph, ON, from 2010 to 2012.
Achievements
Katie Keene plays an instrumental role in leading the clinic site team at Nutrasource. She focuses on creating practical and efficient ways to organize clinical documentation, ensuring subject satisfaction by prioritizing customer service and establishing strong relationships with study subjects. Her contributions enhance the quality and efficiency of clinical trials.