Overview

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In this role, you will support multinational clinical studies by coordinating site activities and ensuring high-quality data. You will work within a cross‑functional team to monitor sites, manage regulatory submissions, and help optimize recruitment. You'll contribute to compliant trial conduct aligned with GCP and ICH standards, impacting patient outcomes and study success.

This is an international, growth‑oriented opportunity with strong support for professional development and a stable, reputable employer.

Responsibilities

Perform site selection, initiation, monitoring and close‑out visits

Support development of a subject recruitment plan

Evaluate quality and integrity of site practices per GCP/ICH

Manage progress by tracking regulatory submissions, recruitment, CRF completion,



and data query resolutions

Collaborate with study site experts and client representatives

Bachelor's Degree and Master's Degree in a scientific discipline or health care

CRA Certification as required by Ministerial Decree dated 15.11.2011

Experience in Pharma Industry and/or Clinical Trials

Very good computer skills including MS Office

Excellent command of English

Strong xkiyazw organizational, time management and problem‑solving skills

Ability to establish and maintain effective working relationships with coworkers, managers, and clients

Flexibility to travel

Driver's license class B

Benefits

Career growth resources

Flexible work schedules

Therapeutic knowledge programs

Company car

Mobile phone

Attractive benefits package

📌 Clinical Research Associate, Sponsor Dedicated - Italy (Milano)
🏢 Altro
📍 Milano