Global Clinical Project Manager

buscojobs España; Salamanca; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Global Clinical Project Manager. This permanent, full-time role involves overseeing clinical trials, managing teams, and ensuring compliance with regulations. Ideal candidates will have strong leadership, project management skills, and experience in clinical trial management. The position is fully home-based, offering a competitive salary and benefits.

Servicios

Health Insurance

Retirement Plans

Wellness Programs

Various Leave Entitlements

Flexible Benefits

Formación

• 6 years' clinical trial management experience.
• Experience managing global or regional virtual teams.

Responsabilidades

• Lead the Study Management Team and provide updates on deliverable status.
• Manage country budgets and monitor expenses.
• Ensure compliance with regulations and participate in audits.

Conocimientos

Leadership

Project Management

Communication

Fluency in English

Educación

BSc in Life Sciences

Herramientas

Microsoft Office

CTMS

TMF systems

Descripción del empleo

As a Global Clinical Project Manager, you will join the world's largest and 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 company, 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.

Responsibilities:

1. Lead the Study Management Team, providing updates on deliverable status.
2. Ensure availability of reports for real-time trial status tracking.
3. Manage documentation and communication of trial progress.
4. Maintain inspection-readiness of the Study Management Team.
5. Act as primary contact for country and regional staff.
6. Partner with the Global Trial Lead to oversee trial activities from planning to close-out.
7. Ensure issue escalation and resolution.
8. Work with the Trial Team to resolve CAPAs timely.
9. Contribute to site selection data collection.
10. Participate in feasibility assessments and provide recommendations.
11. Establish and monitor enrollment commitments and contingency plans.
12. Track and file trial data appropriately.
13. Perform annual quality reviews and ensure document archiving.
14. Manage country budgets and monitor expenses.
15. Oversee vendors and related deliverables.
16. Review and approve vendor invoices and monitor budgets.
17. Create and update trial-specific documents and training materials.
18. Coordinate investigator meetings and establish relationships with stakeholders.
19. Ensure compliance with regulations and participate in audits.
20. Coordinate data cleaning and support database lock processes.
21. Lead process improvements and participate in special initiatives.

Qualifications:

1. BSc in Life Sciences or equivalent; 6 years' clinical trial management experience.
2. Specific therapeutic area experience.
3. Strong knowledge of ICH-GCP and regulations.
4. Proven leadership in managing trials from start-up to closure.
5. Experience managing global or regional virtual teams.
6. Excellent project management and communication skills.
7. Proficiency in Microsoft Office, CTMS, and TMF systems.
8. Monitoring experience preferred.
9. Fluent in local language and English.

What ICON offers:

• Competitive salary and benefits, including health insurance, retirement plans, and wellness programs.
• Various leave entitlements and flexible benefits.
• Inclusive, diverse work environment committed to equality and accessibility.