01 set - Milano
Barrington James
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, collabo
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