Richard Alfaro

Experience

• 

  University of North Carolina

  Sept 2007 - Mar 2015

  Clinical Research Associate

  Performs completion of data forms and data queries for assigned studies; Sample collections, submissions, and tracking; Screening patients, reviewing the eligibility criteria and assuring that time and events for every patient visits are followed as protocol dictates; submission of AE/SAE; Maintain a study binder for each subject containing all the pertinent documents of the study; assist study monitors in overseeing the conduct of the study by providing source documents, discuss, clarify and resolve issues pertaining to the study Show less

• 

  Levine Cancer Institute

  Apr 2015 - now

  Clinical Research Consultant Phase I

  • Completes case report forms, collects source documentation, resolves queries • Conducts study startups and site initiation visits• Maintains regulatory binders, assures study participants are trained in the most recent protocol version/amendment and are included in the 1572 and delegation forms.• Assists research nurse in assessing and obtaining source documentation for patient eligibility, SAE submissions, maintaining AE and con meds log• Maintains study supplies and inventories• Works closely with the study monitor Show less