Experteer Overview
As a Clinical Trial Manager at Medpace in Milan, you lead day-to-day project operations for CNS/Neuroscience studies, collaborating with cross-functional teams to meet study milestones and regulatory requirements. You act as the main Sponsor contact for operational issues and ensure high-quality deliverables. You’ll shape protocols and operational plans while managing risks, vendors, and site quality to help accelerate therapeutic development.
Retribuzione / Benefits
* Manage day-to-day project operations per contract and ICH/GCP rules
* Serve as primary Sponsor contact for operational issues and study deliverables
* Maintain deep knowledge of protocol, therapeutic area, and indication
* Oversee internal project team deliverables and provide necessary training
* Review input for study protocol, edit check specs, data analysis plan, and final report
* Develop operational project plans
* Manage risk assessment and execution
* Oversee study vendors
* Manage site quality and supervise CRAs and monitoring deliverables
Responsabilità
* Bachelor's degree in health or life sciences; advanced degree preferred
* Experience in Phases 1-4 (Phases 2-3 preferred)
* Minimum 2 years of Clinical Trial Management experience; CRO experience preferred
* Experience overseeing project timelines
* Bid defense experience preferred
* Strong leadership skills
Requisiti fondamentali
* Flexible work environment
* Competitive compensation and benefits package
* Competitive PTO packages
* Structured career paths with opportunities for professional growth
* Company-sponsored employee appreciation eventsEmployee health and wellness initiatives
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