Clinical Trial Coordinator

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/78eesf

Experteer Overview In this role you support the clinical research team to run studies in line with GCP, SOPs, and protocols, while respecting budgets and timelines. You own startup activities and document management, ensuring regulatory submissions and site contracts are handled efficiently. You will maintain trial documentation, CTMS updates, and vendor coordination, contributing to audits and reporting. You join a global, collaborative environment that values courage, accountability, and inclusivity to advance clinical research.
Retribuzione / Benefits Oversee startup activities and regulatory submissions at national and international levels under PM oversight
Manage ISF preparation and TMF setup/maintenance under PM oversight
Maintain relationships with Ethics Committees and Competent Authorities
Support sites/vendors invoicing management and tracking




Collaborate on weekly/monthly project reports and update CTMS and trackers
Support CRAs activities follow-up and document translation as needed
Participate in internal, client/sponsor, scientific meetings and audits
Perform additional duties as assigned
Responsabilità Graduation in scientific/health field
Experience in clinical research (CROs, Pharma, or academic/hospital)
Good knowledge of ICH GCP and applicable regulations
Understanding of Clinical Research and Regulatory/Ethical requirements
English proficiency
MS Office Suite proficiency
Strong organizational, multi-tasking, and time management skills
Strong analytical, communication, and interpersonal skills with customer service orientation
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/78eesf