Clinical Trial Manager
15 ore fa
Varese, Lombardia, Italia
Medpace
Tempo pieno
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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
* 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