Senior Clinical Project Manager, Pediatric Oncology

Excelya; Paris; Vor Ort; EUR 90.000 - 130.000; Vollzeit

Zusammenfassung

Excelya is seeking a Senior Clinical Project Manager to oversee international pediatric oncology trials. The role emphasizes leading cross-functional teams, managing timelines, budgets, and quality objectives while ensuring regulatory and ICH-GCP compliance.

You will collaborate with sites, CROs, and vendors to drive study progress, risk mitigation, and governance. Fluent English and strong leadership are essential for success in this global environment.

Qualifikationen

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

Aufgaben

• 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.

Kenntnisse

Clinical project management

ICH-GCP

CRO/vendor management

Budget management

Study timelines

Leadership

English fluent

Ausbildung

Degree in Life Sciences / Pharmacy / Medicine

Jobbeschreibung

Excelya is seeking a Senior Clinical Project Manager to oversee international pediatric oncology trials. The role emphasizes leading cross-functional teams, managing timelines, budgets, and quality objectives while ensuring regulatory and ICH-GCP compliance.

You will collaborate with sites, CROs, and vendors to drive study progress, risk mitigation, and governance. Fluent English and strong leadership are essential for success in this global environment.