Global Clinical Project Manager

ICON; Castellón de la Plana; A distancia; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A leading global clinical research organization is seeking a Global Clinical Project Manager. In this permanent, full-time role, you will lead study management teams, ensure compliance with regulations, and manage vendor relationships. The position requires strong project management skills and a BSc in Life Sciences, along with extensive experience in clinical trials.

Servicios

Health insurance

Retirement plans

Competitive salaries

Leave

Formación

• 6+ years in clinical trial management.
• Strong knowledge of ICH-GCP, laws, and regulations.
• Experience coordinating global or regional teams virtually.

Responsabilidades

• Lead the Study Management Team and manage documentation.
• Ensure compliance with regulations and participate in inspections.
• Manage budgets, vendor oversight, and invoice approvals.

Conocimientos

Project Management

Communication

Analytical Skills

Educación

BSc in Life Sciences

Descripción del empleo

As a Global Clinical Project Manager, you will join the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. This is a permanent, full-time role through ICON on FSP, dedicated to a global pharma, and fully home-based.

You must currently be working as a Global Clinical Project Manager within a CRO or Pharma setting with strong vendor management experience.

What you will be doing :

• Lead the Study Management Team, providing updates on deliverable status.
• Ensure reports are available for real-time trial status tracking.
• Manage documentation and communication of trial progress.
• Maintain inspection-readiness of the Study Management Team.
• Act as the primary contact for Country and Regional staff.
• Partner with the Global Trial Lead to oversee activities from planning to close-out.
• Ensure issue escalation and resolution.
• Work with Trial Team to resolve CAPAs timely.
• Participate in feasibility assessments.
• Establish and monitor enrollment commitments and contingency plans.
• Track and file trial data appropriately.
• Perform Quality Reviews and ensure document archiving.
• Manage budgets, vendor oversight, and invoice approvals.
• Create and update trial-specific documents and training materials.
• Build relationships with internal stakeholders.
• Ensure compliance with regulations and participate in inspections and audits.
• Support protocol expertise and process improvements.
• Lead or participate in special initiatives.

You are :

• BSc in Life Sciences or equivalent, with 6+ years in clinical trial management.
• Experience in specific therapeutic areas.
• Strong knowledge of ICH-GCP, laws, and regulations.
• Proven operational and leadership skills in managing trials.
• Experience coordinating global or regional teams virtually.
• Excellent project management, communication, and analytical skills.
• Proficiency in local language and English.
• Understanding of country-specific budgets and cost drivers.

What ICON can offer you :

We prioritize our people’s well-being and talent development, offering competitive salaries and benefits such as leave, health insurance, retirement plans, and more. We foster a diverse, inclusive culture committed to equal opportunity and accessibility for all candidates.

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