Maria Teresa De Pietro
Clinical Trial Monitor
Clinical Research
Acrylic Designs Inc
Italy
Biography
Maria Teresa De pietro is the Clinical Trial Monitor at CLIOSS S.r.l. Provide operational input into Clinical Projects/Clinical Trials • Develop Monitoring Plan, and have it reviewed and approved by relevant persons • Review Study Manual • Assist in Investigational Site feasibility & selection activities • Assist in collecting information on Investigational Site procedures to request ethical and administrative authorizations • Assist in producing, customizing and collecting documents for Investigational Site activation (e.g. Protocol summary in local languages, Informed Consent Form, Insurance, Questionnaire) • Prepare, perform and follow-up on Pre-study Monitoring Activities, Initiation Monitoring Activities, Monitoring Activities and Close-out Monitoring Activities • Source Document Verification, IMP accountability, ICF review, ICH GCP essential documents review
Research Interest
Clinical Research
