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Clinical Trial Manager

Pubblicato il 13-08-2026 - Iqvia in Italia

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.

We currently offer the exciting opportunity to join the team as Clinical Trial Manager in full-time and work hybrid in Italy (Lombardy). In this role you will be accountable for the operational and scientific oversight, the set-up, execution and delivery of your assigned clinical trials at the local level . working closely together with the Clinical Trial Lead, the CRAs and the regulatory start-up team in the assigned trial.
Key Responsibilities
- Accountable for the operational and scientific oversight, the set-up, execution and delivery of their assigned clinical trials at the local level.



CTMs contribute to delivery of sponsor´s pipeline through accurate planning and efficient execution of trials that bring speed & value to participating patients and sites
- Provides leadership and direction to the Operational Unit trial team and is accountable for the overall success and delivery of their assigned clinical trial/s according to defined milestones and key performance indicators
- Responsible for steering and directing clinical trial activities, including patient and site engagement activities and interaction with multiple internal and external stakeholders and trial team members at a local and global level
- Responsible for managing the planning, implementation and tracking of the clinical trial process as well as risk mitigation. The CTM serves as a proactive member of the trial team, liaising closely with the Clinical Trial Leader (“CTL”) on all study-related issues

Trial Preparation, Conduct And Closeout
- Accountable for the trial activities for responsible R/OPU
- Verify the trial is conducted in compliance with GCP

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