Experteer Overview

Le seguenti informazioni hanno lo scopo di fornire ai potenziali candidati una migliore comprensione dei requisiti per questo ruolo.

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

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

Responsabilità

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 xlwpduy 2-3 preferred)

Management of overall project timeline

Strong leadership skills

Bid defense experience preferred

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 events

Employee health and wellness initiatives

📌 Clinical Trial Manager - Italy - Neuroscience / Ophthalmology (Roma)
🏢 Altro
📍 Roma