Clinical Project Manager

Barrington James; Milano; In loco; EUR 60.000 - 80.000; Tempo pieno

Descrizione del lavoro

A leading clinical research organization is seeking an experienced Clinical Project Manager in Milan, Italy. The role involves leading clinical trial execution, managing resources, and ensuring compliance with regulations. The ideal candidate has over 5 years of clinical research experience, including project management. This position offers competitive salary, performance bonuses, and opportunities for career growth.

Servizi

Competitive salary

Performance bonus

Comprehensive benefits package

Competenze

• 5+ years of experience in clinical research, with a minimum of 2 years in project management.
• Fluency in Italian and English, both written and spoken.
• Strong understanding of ICH-GCP and EU regulatory requirements.

Mansioni

• Lead and oversee the execution of clinical trials across Italy.
• Manage timelines, budgets, and resources for projects.
• Serve as the primary liaison between sponsors and internal teams.

Conoscenze

Project management

Clinical research

Leadership

Communication

Problem-solving

Vendor management

Formazione

Bachelor’s or Master’s degree in Life Sciences

Descrizione del lavoro

Clinical Project Manager – Italy

Location: Milan, Italy

Department: Clinical Operations / Project Management

Employment Type: Full-time / Permanent

About the Role

We are seeking an experienced and proactive Clinical Project Manager (CPM) to lead and oversee the execution of clinical trials across Italy. Based in Milan, this position is responsible for the overall management and delivery of clinical projects, ensuring quality, compliance, and operational excellence throughout the study lifecycle.

The CPM will serve as the main point of contact for internal teams, sponsors, and investigative sites, driving projects forward to meet milestones and deliverables on time and within budget.

Key Responsibilities

• Plan, initiate, execute, and close out clinical studies in accordance with ICH-GCP, local regulations, and company SOPs.
• Manage timelines, budgets, and resources, ensuring projects remain on track and within scope.
• Oversee site selection, startup, monitoring progress, and study closure activities.
• Coordinate cross-functional teams, including clinical operations, regulatory affairs, data management, and quality assurance.
• Serve as the primary liaison between sponsors, investigators, vendors, and internal stakeholders.
• Track project performance, prepare progress reports, and elevate risks or issues when needed.
• Mentor and support CRAs and other team members as appropriate.
• Contribute to process improvements and best practices within Clinical Operations.

Qualifications & Experience

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
• Minimum 5 years of experience in clinical research, including at least 2 years in project management.
• Strong understanding of ICH-GCP, EU and Italian regulatory requirements, and clinical trial operations.
• Proven ability to manage multiple studies and teams concurrently.
• Fluent in Italian and English (written and spoken).
• Excellent communication, leadership, and problem-solving skills.
• Experience with vendor and budget management.
• Willingness to travel within Italy and occasionally across Europe.

Why Join Us?

Be part of a collaborative, forward-thinking organization committed to advancing clinical research.

Enjoy a dynamic, supportive environment that values initiative and innovation.

Competitive salary, performance bonus, and comprehensive benefits package.

Milan-based position with opportunities for career growth and leadership development.