04 set - Milano
Altro
Location: Milan, Italy (Hybrid/Home-Based)
Employment Type: Permanent, Full-Time
About the Opportunity
Our client is a well-established global Contract Research Organisation (CRO) with a strong reputation for delivering high-quality clinical trials across a broad range of therapeutic areas. Due to continued growth within their oncology portfolio, they are seeking an experienced Clinical Research Associate to support Phase II–IV studies, with a particular focus on Solid Tumour Oncology .
This is an excellent opportunity to join an organisation that offers long‐term career development, exposure to innovative oncology studies and a collaborative working environment.
Key Responsibilities
Independently manage investigative sites across Northern Italy.
Conduct Site Selection, Site Initiation, Monitoring and Close-Out Visits.
Ensure studies are conducted in accordance with ICH-GCP, protocol requirements and applicable regulatory guidelines.
Build strong relationships with investigators and site personnel.
Monitor patient recruitment, data quality and protocol compliance.
Review source documentation and resolve data queries.
Support study timelines whilst maintaining the highest quality standards.
Collaborate closely with Clinical Trial Managers and cross-functional project teams.
Requirements
Minimum 3 years of independent CRA monitoring experience within a CRO, sponsor or biotech environment.
Strong experience monitoring Solid Tumour Oncology clinical trials.
Good understanding of ICH-GCP and European clinical trial regulations.
Experience across Phase II–IV clinical studies is advantageous.
Excellent organisational and communication skills.
Ability to work independently while managing multiple priorities.
Fluent Italian and English.
What's on Offer
Competitive salary and comprehensive benefits package.
Opportunity to work on innovative oncology programmes.
Career progression within an established global CRO.
Supportive, collaborative and international working environment.
Flexible home-based working with regional site monitoring.
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