Global Clinical Project Manager

ICON; España; A distancia; EUR 60.000 - 100.000; Jornada completa

Descripción de la vacante

Join a leading global clinical research organization as a Global Clinical Project Manager. In this exciting full-time role, you will lead the Study Management Team, ensuring effective trial management and compliance with regulations. You will leverage your extensive experience in clinical trial management and vendor oversight to drive project success. This home-based position offers competitive salaries and benefits, fostering a diverse and inclusive culture. If you're passionate about improving healthcare through innovative research, this opportunity is perfect for you.

Servicios

Health Insurance

Retirement Plans

Leave Benefits

Formación

• 6+ years in clinical trial management with strong leadership skills.
• Proven operational skills in managing trials and coordinating teams.

Responsabilidades

• Lead the Study Management Team and ensure trial progress tracking.
• Manage budgets, vendor oversight, and ensure compliance with regulations.

Conocimientos

Clinical Trial Management

Vendor Management

Project Management

Communication Skills

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 :

1. Lead the Study Management Team, providing updates on deliverable status.
2. Ensure reports are available 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 the primary contact for Country and Regional staff.
6. Partner with the Global Trial Lead to oversee activities from planning to close-out.
7. Ensure issue escalation and resolution.
8. Work with Trial Team to resolve CAPAs timely.
9. Support site selection data collection.
10. Participate in feasibility assessments.
11. Establish and monitor enrollment commitments and contingency plans.
12. Track and file trial data appropriately.
13. Perform Quality Reviews and ensure document archiving.
14. Manage budgets, vendor oversight, and invoice approvals.
15. Create and update trial-specific documents and training materials.
16. Coordinate Investigator Meetings.
17. Build relationships with internal stakeholders.
18. Ensure compliance with regulations and participate in inspections and audits.
19. Coordinate data cleaning for database lock.
20. Support protocol expertise and process improvements.
21. Lead or participate in special initiatives.

You are :

1. BSc in Life Sciences or equivalent, with 6+ years in clinical trial management.
2. Experience in specific therapeutic areas.
3. Strong knowledge of ICH-GCP, laws, and regulations.
4. Proven operational and leadership skills in managing trials.
5. Experience coordinating global or regional teams virtually.
6. Excellent project management, communication, and analytical skills.
7. Proficiency in local language and English.
8. 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.