17 set - Milano
Medpace
Overview In this role you will manage day-to-day clinical trial operations and serve as the primary sponsor contact. You’ll apply your CNS/Neuroscience expertise or broaden to other areas while ensuring compliance with ICH/GCP and regulatory standards. You’ll lead cross-functional teams, oversee vendors and sites, and contribute to protocol and study deliverables.
This position sits in Medpace’s Clinical Trial Management Group in Milan, offering flexibility after probation and a strong focus on impact through global trial execution.
Retribuzione / Benefits
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Responsabilità
- Oversee day-to-day trial operations per contract and regulatory requirements
- Act as primary Sponsor contact for operational issues and study deliverables
- Maintain deep knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight and ensure training for project team members
- Review and provide input on protocol, edit check specs, and data analysis plans
- Develop operational project plans and manage risk and vendor relationships
- Supervise site quality and monitor deliverables by Clinical Research Associates
Requisiti fondamentali
- Bachelor’s degree in a health or life science-related field
- Minimum 2 years of Clinical Trial Management experience
- CRO experience preferred
- Experience in Phases 1-4 (Phases 2-3 preferred)
- Management of overall project timeline
- Strong leadership skills
- Bid defense experience preferred
- leadership
- cross-functional collaboration
- problem solving
- ICH/GCP knowledge
- study protocol review
- data analysis plan input
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