Senior Global Pediatric Oncology Project Lead

Excelya; Paris; On-site; EUR 70,000 - 100,000; Full time

Job summary

Excelya is seeking a Senior Clinical Project Manager to oversee the operational management of an international pediatric oncology trial. You will lead cross-functional teams, manage study timelines and budgets, and ensure adherence to ICH-GCP and regulatory standards.

The role emphasizes collaboration, study governance, and continuous process improvement, with a focus on risk management, stakeholder engagement, and delivery of high-quality trial outcomes. Fluency in English is required.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Project leadership

Stakeholder management

Communication

English (Fluent)

Education

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

Job description

Excelya is seeking a Senior Clinical Project Manager to oversee the operational management of an international pediatric oncology trial. You will lead cross-functional teams, manage study timelines and budgets, and ensure adherence to ICH-GCP and regulatory standards.

The role emphasizes collaboration, study governance, and continuous process improvement, with a focus on risk management, stakeholder engagement, and delivery of high-quality trial outcomes. Fluency in English is required.