Clinical Research Associate

Barrington James; Milano; Ibrido; EUR 42.000 - 64.000; Tempo pieno

Vantaggi offerti da questo lavoro

Comprehensive benefits package

Flexible home-based working

International environment

Descrizione del lavoro

Barrington James is seeking a Clinical Research Associate to support Phase II–IV solid tumour oncology trials across Northern Italy, with a hybrid/home-based working arrangement. The role emphasizes site management, regulatory compliance, and collaboration with cross-functional teams.

Ideal candidates will have at least 3 years of independent CRA monitoring experience, fluent Italian and English, and strong knowledge of ICH-GCP and European trial regulations.

Competenze

• Minimum 3 years of independent CRA monitoring experience.
• Strong experience monitoring Solid Tumour Oncology trials.
• Good understanding of ICH-GCP and European clinical trial regulations.

Mansioni

• Independently manage investigative sites across Northern Italy.
• Conduct Site Selection, Site Initiation, Monitoring and Close-Out Visits.
• Ensure studies comply with ICH-GCP and 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.
• Collaborate with Clinical Trial Managers and cross-functional teams.

Conoscenze

Site monitoring

Study coordination

Communication

Fluent Italian & English

Formazione

Bachelor's degree in life sciences

Strumenti

CTMS

EDC

Descrizione del lavoro

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.