Naturopathic Medical Doctor and Clinical Investigator

• Jul 2020 - Present

Naturopathic Medical Doctor

• May 2019 - Jul 2020

Naturopathic Physician

• Jun 2017 - May 2019

Director of Genetic Services

• Apr 2017 - May 2017

AGS empowers its clients to improve their health by making informed lifestyle choices based on their unique genes. We analyze clients’ unique DNA and provide actionable data that tailors medication, nutrition, diet and exercise choices that best optimize their health. Results from the AGS Health and Wellness report can help improve multiple phases of everyday lives: -Boost Energy -Enhance Vitality -Increase Muscle and Bone Health -Control Weight and Eating Behaviors -Optimize Exercise Routine -Identify Vitamin Deficiencies -Improve Mood Results from the AGS Drug Sensitivity test can: -Save patient lives by avoiding adverse drug reactions -Simplify a complex process of choosing medication by prescribing based on genetics -Get patient on the right medication at the right dose based on their genes -Reduce trial and error of medication choices -Save patients money with medication changes -Help provide the intended therapeutic benefit with limited side effects Show less

Clinical Research Coordinator

• May 2014 - Apr 2017

• Responsible for coordinating and implementing research protocols; assumes primary responsibility for sponsor relationships and the execution and management of new clinical trials • Collaborate with finance committee to prepare proposed trial budgets • Present successful recruitment and retention strategies at sponsor conferences • Serve as the main contact for patients and families who are engaged in clinical studies: assist in recruitment and screening of participants, obtain medical history, explain procedures and consent forms; perform EKG and cognitive assessments, collect vital signs and other data as required by protocol and assist in interpreting and evaluating results • Departmental responsibility to utilize “Certificate to Dispense” license to verify and sign off on proper investigational medication dosage and administration • Ensure uniform implementation of protocols, assist in preparing materials for IRB submission, communicate with study investigators regarding adverse events and medical follow up • Responsible for ensuring quality control of the data and protocol compliance • Provide leadership and guidance by training assistants within the clinical trials department Show less