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This webinar will identify areas where Principal Investigators (PIs) commonly make mistakes during clinical trials. Each “pitfall” will be highlighted to describe areas often overlooked or under emphasized by PIs at investigative sites.

Topics Include:

  • Delegation of Study-Related Tasks
  • Training
  • Supervision of the Conduct of an Ongoing Clinical Trial
  • Protocol Adherence
  • Live Q & A Session

About the Presenter:

Alia Legaux, D.H.Sc., M.Ed., MCHES, CCRP
GCP Senior Auditor
USDM Life Sciences

  • Worked as an Investigator for the Food and Drug Administration (FDA) for 5.5 years
  • Contributed as a member of the International Inspection Cadre at FDA
  • Experienced auditor with over 13 years of experience in the clinical research industry
Alia Legaux

D.H.Sc., M.Ed., MCHES, CCRP, GCP Senior Auditor USDM Life Sciences Worked as an Investigator for the Food and Drug Administration (FDA) for 5.5 years Contributed as a member of the International Inspection Cadre at FDA Experienced auditor with over 13 years of experience in the clinical research industry

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