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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