CRA (臨床開発モニター)経験者/ IQVIA Services
Core
Conduct clinical monitoring activities (site selection, initiation, monitoring, close-out) based on monitoring management plans to ensure case report forms meet quality standards and adverse events are managed.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data quality and patient safety
Domain
Clinical Research / Life Sciences
Required skills
GCP knowledge, Site monitoring, Case report form review, Adverse event reporting, Site selection, Initiation visits, Close-out visits
Preferred skills
Oncology experience, Global project experience, University hospital experience, Mentoring new staff
Technologies
None stated
Responsibilities
Perform site selection, initiation, monitoring and close-out visits; Conduct SDV and create monitoring reports; Confirm and manage adverse events in patients.
Seniority
Mid-Senior, hands-on IC
