Global Clinical Project Manager

Pharmaceutical Research Associates, Inc; Murcia; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

Join a leading global clinical research organization as a Global Clinical Project Manager. This fully home-based, permanent role requires strong vendor management and leadership skills. You will oversee trial operations from start-up to closure, ensuring compliance and effective stakeholder management while contributing to process improvements.

Servicios

Competitive salaries

Benefits focused on well-being

Work-life balance

Formación

• 6 years of clinical trial management experience.
• Experience in specific therapeutic areas.

Responsabilidades

• Lead the Study Management Team and provide updates.
• Ensure compliance with regulations and participate in inspections.
• Manage documentation and communication of trial progress.

Conocimientos

Leadership

Stakeholder Management

Project Planning

Analytical Skills

Communication

Educación

BS degree in Life Sciences

Herramientas

Microsoft applications

Descripción del empleo

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

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

Responsibilities

What you will be doing :

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. Serve as primary contact for Country and Regional staff.
6. Partner with the Global Trial Lead from planning to trial close-out.
7. Escalate issues and drive resolution.
8. Ensure timely CAPA resolution and contribute as CAPA owner or contributor.
9. Support site selection through 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 proper archiving.
14. Establish and monitor country budgets and vendor oversight.
15. Review and approve vendor invoices and monitor expenditures.
16. Create and update trial-specific documents and training materials.
17. Coordinate Investigator Meetings and maintain stakeholder relationships.
18. Ensure compliance with regulations and participate in inspections and audits.
19. Coordinate data cleaning and support database lock.
20. Contribute to process improvements and participate in initiatives.

Qualifications

You are :

1. BS degree or equivalent in Life Sciences with 6 years of clinical trial management experience.
2. Experience in specific therapeutic areas.
3. Strong knowledge of ICH-GCP, local laws, and regulations.
4. Proven leadership in managing trial operations from start-up to closure.
5. Effective stakeholder management and team leadership skills.
6. Experience coordinating global or regional teams in a virtual environment.
7. Excellent project planning and management skills.
8. Proficient in Microsoft applications and clinical trial systems.
9. Experience or knowledge in monitoring, data management, or central monitoring.
10. Fluent in local language and English, with excellent communication skills.
11. Strong analytical skills and ability to manage ambiguity.
12. Experience developing presentations and engaging stakeholders.
13. Understanding of country-specific budgeting and cost drivers.

What ICON can offer you: Our success depends on the quality of our people. We’ve built a diverse culture that rewards high performance and nurtures talent, offering competitive salaries and benefits focused on well-being and work-life balance.