Clinical Research Associate
IQVIA
Aug 2016 - Jul 2021 (5 years)
Performing Clinical Monitoring Activities, Site Selection, Site Initiation, Site Monitoring, and Close
Out. Provide support for study start-up in ICF customization and Initial Clinical Trial Application
Submission. Site Management of the study site such as Amendment of the trial agreement,
collecting and maintaining eTMF document, management of action items, communication with
the study team and sites, management of revised clinical trial document, study site staff training,
and IP management.
CRA oversight of 1 site of Phase IIIb Diphtheria, Tetanus, Pertussis, Hepatitis B, Poliomyelitis,
Haemophilus Influenza, Type b Infection trials, 4 sites of Phase II Gastric or Gastroesophageal
Junction Adenocar