Experience

TGen - Part of City of Hope

• United States
• Biotechnology Research
• 200 - 300 Employee

• Sr Research Compliance Specialist

  • May 2017 - Present

  - Manage a portfolio of 60+ biospecimen protocols for the institute - Complete Quality Assurance audits of open protocols - Aid investigators with protocol design, design study documents, and complete all IRB submissions. - Manage a portfolio of 60+ biospecimen protocols for the institute - Complete Quality Assurance audits of open protocols - Aid investigators with protocol design, design study documents, and complete all IRB submissions.



Southwest Kidney Institure

• Tempe, Arizona

• Clinical Research Coordinator

  • Aug 2016 - May 2017

  Coordinated 3 concurrent clinical device trials between two high enrolling sites at Southwest Kidney Institute. • Screened clinic patients for study eligibility and enrolled participants in study. • Managed financial compensation and clinical follow-up with participants • Worked with study sponsor to ensure accurate days collection and adverse event reporting. Coordinated 3 concurrent clinical device trials between two high enrolling sites at Southwest Kidney Institute. • Screened clinic patients for study eligibility and enrolled participants in study. • Managed financial compensation and clinical follow-up with participants • Worked with study sponsor to ensure accurate days collection and adverse event reporting.



Arizona State University

• United States
• Higher Education
• 700 & Above Employee

• Graduate Research Assistant

  • Sep 2015 - May 2017

  Performed many project management duties for several different projects under Dr. Jeffrey La Belle. • Acted as liaison between La Belle laboratory and the Mayo Clinic to coordinate sample testing for a clinical trial and presented end of study data to physicians. • Aided in writing several grants, including NIH, NSF, DOD, and industry proposals. • Responsible for writing IRB applications and submitting modifications or continuing reviews for several projects in the lab. • Designed a 10 subject clinical trial for testing a wearable device. Aided in the design of a 30 subject, 30-day clinical trial for next generation device validation.