Global Pediatric Oncology Clinical Project Lead

Excelya; Paris; Presencial; EUR 90.000 - 120.000; Jornada completa

Descripción de la vacante

Excelya is seeking a Senior Clinical Project Manager to support the operational management of an international pediatric oncology trial. You will lead cross-functional teams, oversee timelines, budgets and quality objectives, and manage relationships with sites, CROs and vendors.

This role requires a strong knowledge of ICH-GCP and regulatory requirements, excellent communication, and a proven ability to deliver studies on time in a global setting.

Formación

• Degree in Life Sciences, Pharmacy, Medicine, or related field.
• Significant experience in Clinical Project Management within clinical research.
• Strong knowledge of international trials and ICH-GCP guidelines.
• Experience managing CROs, vendors, budgets and study timelines.
• Desirable: oncology and/or pediatric clinical studies.
• Excellent communication, stakeholder management and leadership.
• Fluent in English.

Responsabilidades

• Lead and coordinate the operational conduct of international clinical studies.
• Oversee study timelines, milestones, budget, and quality objectives.
• Manage relationships with investigational sites, CROs, vendors, and study stakeholders.
• Ensure compliance with ICH-GCP, regulatory requirements, and study procedures.
• Monitor study progress, patient recruitment, and site performance.
• Identify risks and implement mitigation plans to ensure successful study delivery.
• Coordinate cross-functional teams and facilitate project governance meetings.
• Contribute to study reporting, inspection readiness, and continuous process improvement.

Conocimientos

Leadership

Stakeholder management

Communication

English fluency

Educación

Degree in Life Sciences, Pharmacy, Medicine, or related field

Descripción del empleo

Excelya is seeking a Senior Clinical Project Manager to support the operational management of an international pediatric oncology trial. You will lead cross-functional teams, oversee timelines, budgets and quality objectives, and manage relationships with sites, CROs and vendors.

This role requires a strong knowledge of ICH-GCP and regulatory requirements, excellent communication, and a proven ability to deliver studies on time in a global setting.