Experienced Clinical Research Associate, Home based
OverviewIn this role you join Medpace's Clinical Monitoring team in Italy to perform site-based monitoring activities for clinical studies. You will receive comprehensive training and work either remotely or from an office, contributing to study integrity and regulatory compliance. You collaborate with site staff and cross-functional teams to ensure quality data and patient safety, with opportunities for career growth in a global CRO. This position offers meaningful impact by supporting efficient, compliant clinical development.
Retribuzione / Benefits
Flexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
Responsabilità
Conduct qualification, initiation, monitoring and closeout visits at research sites per protocolCommunicate with site staff, coordinators and clinical research physiciansVerify investigator qualifications, training,
facilities and resourcesVerify data through source documentation checks and ensure good documentation practicesEnsure eligibility of enrolled subjects and perform regulatory document reviewManage regulatory documents and accountability for investigational products/devicesReview adverse events and related data to ensure accurate reportingAssess site patient recruitment/retention and suggest improvementsPrepare monitoring reports and follow-up letters summarizing findings and recommended actions
Requisiti fondamentali
Master degree in health-related fieldCRA certification completed per DMC 15/11/2011Previous experience as CRAWillingness to travel 60-80% nationallyFamiliarity with Microsoft OfficeFluent in English and ItalianStrong communication skillsPresentational abilitiesTeam collaborationMicrosoft OfficeRegulatory document reviewGCP/compliance knowledge
Retribuzione / Benefits
Flexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
Responsabilità
Conduct qualification, initiation, monitoring and closeout visits at research sites per protocolCommunicate with site staff, coordinators and clinical research physiciansVerify investigator qualifications, training,
facilities and resourcesVerify data through source documentation checks and ensure good documentation practicesEnsure eligibility of enrolled subjects and perform regulatory document reviewManage regulatory documents and accountability for investigational products/devicesReview adverse events and related data to ensure accurate reportingAssess site patient recruitment/retention and suggest improvementsPrepare monitoring reports and follow-up letters summarizing findings and recommended actions
Requisiti fondamentali
Master degree in health-related fieldCRA certification completed per DMC 15/11/2011Previous experience as CRAWillingness to travel 60-80% nationallyFamiliarity with Microsoft OfficeFluent in English and ItalianStrong communication skillsPresentational abilitiesTeam collaborationMicrosoft OfficeRegulatory document reviewGCP/compliance knowledge