Global Clinical Project Manager

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

Descripción de la vacante

A leading global clinical research organization is seeking a Global Clinical Project Manager to oversee trial activities from planning to close-out. This fully home-based, full-time role requires strong leadership and vendor management skills, along with significant experience in clinical trial management within a CRO or Pharma setting. The successful candidate will play a critical role in ensuring the success of clinical trials and maintaining compliance with regulations.

Servicios

Health Insurance

Retirement Plans

Flexible Benefits

Employee Assistance Programme

Life Assurance

Formación

• At least 6 years of clinical trial management experience in pharma or CRO.
• Experience in coordinating global or regional teams in virtual environments for 2-3 years.

Responsabilidades

• Lead the Study Management Team and provide updates on deliverable status.
• Manage documentation and communication of trial progress.
• Ensure protocol compliance and participate in inspections and audits.

Conocimientos

Leadership

Stakeholder Management

Project Management

Risk Mitigation

Communication

Analytics

Educación

BS degree in Life Sciences

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. 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. Escalate and resolve issues promptly.
8. Ensure CAPAs are addressed timely; act 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. Ensure proper tracking and filing of trial documents.
13. Perform annual quality reviews and archive documents per requirements.
14. Manage country budgets, monitor expenses, and oversee vendor deliverables.
15. Review and approve vendor invoices and monitor trial budgets.
16. Create and update trial-specific documents and training materials.
17. Coordinate Investigator Meetings and maintain stakeholder relationships.
18. Ensure protocol compliance and participate in inspections and audits.
19. Coordinate data cleaning and support database lock processes.
20. Contribute to process improvements and participate in initiatives.

Qualifications

You are:

1. Holding a BS degree or equivalent in Life Sciences with at least 6 years of clinical trial management experience in pharma or CRO.
2. Having specific therapeutic area experience.
3. Well-versed in ICH-GCP, local laws, and regulations.
4. Possessing strong operational knowledge and a successful track record in managing trials.
5. Demonstrating effective leadership and stakeholder management skills.
6. Experienced in coordinating global or regional teams in virtual environments for at least 2-3 years.
7. Proficient in project management, risk mitigation, and IT systems related to clinical trials.
8. Fluent in local language(s) and English, with excellent communication skills.
9. Strong in analytics, ambiguity management, and presentation skills.

What ICON can offer you: Our success depends on our people. We prioritize diversity, high performance, and talent development. Benefits include various leave entitlements, health insurance, retirement plans, an Employee Assistance Programme, life assurance, and flexible benefits tailored to each country. Visit our careers site to learn more about working at ICON and our commitment to diversity and inclusion.