Global Clinical Project Manager

Pharmaceutical Research Associates, Inc; Logroño; A distancia; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

Join a leading global clinical research organization as a Global Clinical Project Manager. In this full-time, home-based role, you'll lead study management teams, ensuring compliance and quality throughout clinical trials. Your expertise in vendor management and project coordination will drive success in a diverse and inclusive environment. With a strong focus on professional development, this opportunity allows you to contribute to innovative healthcare solutions while enjoying a comprehensive benefits package tailored to your needs. If you're passionate about improving patient outcomes and thrive in a dynamic setting, this role is perfect for you.

Servicios

Annual Leave

Health Insurance

Retirement Plans

Employee Assistance Program

Life Assurance

Flexible Benefits

Formación

• 6+ years in clinical trial management within pharma or CRO.
• Strong knowledge of ICH-GCP and local regulations.

Responsabilidades

• Lead the Study Management Team and ensure trial progress.
• Manage budgets, monitor expenses, and review vendor invoices.
• Coordinate data cleaning and support database lock.

Conocimientos

Clinical Trial Management

Vendor Management

Project Management

Communication Skills

Analytical Skills

Educación

BSc in Life Sciences

Herramientas

Microsoft Office

TMF

CTMS

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, 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 to support real-time trial 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. Coordinate CAPAs and contribute to data collection for site selection.
9. Participate in feasibility assessments.
10. Establish and monitor enrollment commitments and contingency plans.
11. Track and file trial data appropriately.
12. Perform Quality Reviews and ensure proper archiving.
13. Manage budgets, monitor expenses, and review vendor invoices.
14. Create and update trial-specific documents and training materials.
15. Coordinate Investigator Meetings and maintain stakeholder relationships.
16. Ensure compliance with regulations and participate in audits.
17. Coordinate data cleaning and support database lock.
18. Lead process improvements and special initiatives.

Qualifications

1. BSc in Life Sciences or equivalent; 6+ years in clinical trial management within pharma or CRO.
2. Experience in specific therapeutic areas.
3. Strong knowledge of ICH-GCP, local laws, and regulations.
4. Proven leadership and team management skills.
5. Experience in coordinating global or regional teams virtually.
6. Excellent project management and communication skills.
7. Proficiency with Microsoft Office, TMF, CTMS, and willingness to learn new systems.
8. Monitoring experience or related fields such as data management.
9. Fluency in local language and English.
10. Strong analytical skills and ability to manage ambiguity.
11. Experience in developing presentations and stakeholder communication.
12. Knowledge of country-specific budgeting and cost drivers.

What ICON Offers

We value our people and offer a range of benefits including annual leave, health insurance, retirement plans, Employee Assistance Program, life assurance, and flexible benefits tailored to each country. We are committed to diversity and inclusion, providing a workplace free from discrimination and harassment. We encourage all qualified candidates to apply, even if they do not meet every requirement.