Overview In this role, you will lead the Study Management Team to coordinate global clinical operations for both in‐house and outsourced trials. You ensure timely delivery of study milestones, oversee country/site activities, and maintain inspection readiness across GCDO. You partner with the Global Trial Lead and act as a primary contact for country/regional teams and CROs. You shape trial planning, risk mitigation, and quality oversight, contributing to the sponsor's regulatory and data integrity goals. This is a chance to drive global collaboration and process improvement in a complex, fast‐paced environment.
Responsibilities Lead the Study Management Team and provide status updates to trial members
Ensure real‐time trial status reporting and documentation of progress
Maintain inspection readiness and compliance with SOPs, GCP, and regulations
Act as primary contact for country and regional staff and for local GCDO teams
Coordinate central activities from planning to close‐out with the Global Trial Lead




Escalate issues and drive CAPA resolution as CAPA owner or contributor
Support site selection, feasibility, enrollment planning, and vendor oversight including budgets
Develop trial‐specific documents and training materials; support Investigator Meetings
Qualifications BS degree or equivalent in Life Sciences
6–8 years of clinical trial management experience in pharma or CRO
Strong knowledge of ICH‐GCP, local laws and regulations
Proven leadership to drive SMT and manage stakeholders
Experience coordinating global/regional teams in a virtual environment
Proven ability to plan, manage risk, and drive projects to database lock and close‐out
Strong IT skills, CTMS, TMF, and willingness to learn new systems
Travel flexibility and proficiency in local language and English
Excellent communication and decision‐making abilities
Experience with budgeting, vendor management, and submission support
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📌 Global Senior Trial Delivery Manager (Italia)
🏢 Altro
📍 Italia