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Free-lance with over 25 years of experience in medical dept of pharmaceutical industries and global/national CROs


Self Assessment :
CollaborationCompetitivenessEfficiencyFlexibilityInterest in knowledgeProblem solvingResult OrientedService orientedAttention to detail


Self Assessment :
Clinical researchClinical monitoringClinical Study DesignCMC Regulatory AffairsContract negotiationCROData entry

Skills and Expertise

Self Assessment :
Develop clinical trial protocols Monitor a clinical studyAdverse event reportingCollaborate with PI and institution to respond to any audit findings and implement-approved recommendations.Create clinical project documents according to the protocolData entryIdentify investigatorsInteract with ethics committeeManage Clinical Trial Management System (CTMS) Monitor dataMonitoring enrolmentNegotiate budget Negotiate protocol details Pre-study procedures Regulatory submissionsRegulatory documentationReport serious adverse events (SAE)Resolves queriesRespond to audit findingsSchedule trial visitsSelect investigatorsSite management


  • degree in Pharmaceutica chemistry from university of Milan in 1978

Training and Certification

  • Clinical research associtae in 2016 Certification
  • Chemistry professor in 2000 Certification
  • Pharmacist in 1980 Certification


BrightOwl Assessment:
Self Assessment:

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Senior Consultant Regulatory and Start-Up Specialist Regulatory Affairs Consultant Senior Clinical Research Associate (CRA)
  • Positions I am NOT interested in:
    BioStatistician Clinical Trial Assistant (CTA) Freelance Science Writer Data Architect
  • Work From Home:
  • Work Regime:
    BrightOwl freelancer :    30-36 Hours per week :    5% Free Per Month(in coming months)
  • International:

Area / Region

Prato, PO, Italia


Driving License
  • Yes