Experience

OnPoint Clinical Staffing Services

• United States
• Staffing and Recruiting
• 1 - 100 Employee

• Senior Regional Clinical Research Associate

  • Jun 2022 - Present

  Perform all aspects of clinical monitoring and site management in accordance with ICH-GCP, FDA guidelines, local regulations, and company SOPs. Conduct onsite and remote monitoring visits to assess protocol and regulatory compliance. Manage clinical research sites and clinical trial documentation. Utilize CTMS, TMF, and EDC platforms. Perform all aspects of clinical monitoring and site management in accordance with ICH-GCP, FDA guidelines, local regulations, and company SOPs. Conduct onsite and remote monitoring visits to assess protocol and regulatory compliance. Manage clinical research sites and clinical trial documentation. Utilize CTMS, TMF, and EDC platforms.



Chiltern

• Pharmaceutical Manufacturing
• 400 - 500 Employee

• Senior Clinical Research Associate

  • Mar 2016 - Present



UBC - An Express Scripts Company

• Senior Clinical Research Associate

  • Jul 2012 - Present



PPD

• United States
• Research Services
• 700 & Above Employee

• Senior Clinical Research Associate-SSU

  • Aug 2010 - Jul 2012



Novum Pharmaceutical Research Services

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Clinical Research Associate I/II

  • Sep 2007 - Aug 2010