Experience

FHI Clinical Inc.

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Vice President, Global Strategy

  • Apr 2019 - Present



FHI 360

• United States
• International Trade and Development
• 700 & Above Employee

• Director, Clinical Operations

  • Oct 2016 - Mar 2019

• Associate Director, Clinical Research

  • Aug 2006 - Sep 2016

  Help with the development of protocols and review protocols and study-related materials for assigned clinical research studies; coordinate study implementation of multi-center and multi-country trials in Africa; participate in study monitoring; and ensure that research is conducted within the requirements of their protocols and in accordance with applicable regulations and guidelines. Supervise and mentor the Africa Regional Clinical Research Unit.

• Senior Clinical Research Manager

  • Dec 2004 - Aug 2006

  Helped with the development of protocols and reviews protocols and study-related materials for assigned clinical research studies; coordinated study implementation; participated in study monitoring; and ensured that research is conducted within the requirements of their protocols and in accordance with applicable regulations and guidelines.



inVentiv Health Clinical

• United States
• Pharmaceutical Manufacturing
• 500 - 600 Employee

• Clinical Research Associate II

  • Feb 2004 - Nov 2004

  Monitored Clinical trials in the US and Canada. Monitored Clinical trials in the US and Canada.



PPD

• United States
• Research Services
• 700 & Above Employee

• Clinical Research Associate III

  • Jan 2001 - Jan 2004

  Participated in multiple multi-center clinical research studies; assisted with project data clinical review and management; presented at investigator meetings for assigned studies; monitored sites according to applicable SOPs and FDA guidelines; reviewed case report forms for adherence to protocol requirements; resolved CRF discrepancies; and performed drug accountability. Participated in multiple multi-center clinical research studies; assisted with project data clinical review and management; presented at investigator meetings for assigned studies; monitored sites according to applicable SOPs and FDA guidelines; reviewed case report forms for adherence to protocol requirements; resolved CRF discrepancies; and performed drug accountability.



Labcorp

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Medical Technologist

  • Jan 2000 - Jan 2001

  Part-time medical technologist. Part-time medical technologist.



The US Oncology Network

• Hospitals and Health Care
• 700 & Above Employee

• Data Coordinator

  • Jan 1999 - Jan 2001

  Collected, reviewed, and completed clinical research patient data from sites participating in research studies; ensured the quality of study data; interacted with study sponsors, investigators, and site coordinators to identify and address protocol deviations; collected source documentation for FDA purposes; and participated in all phases of clinical trials. Collected, reviewed, and completed clinical research patient data from sites participating in research studies; ensured the quality of study data; interacted with study sponsors, investigators, and site coordinators to identify and address protocol deviations; collected source documentation for FDA purposes; and participated in all phases of clinical trials.