Senior International Clinical PM — Pediatric Oncology

Excelya Group; Paris; Vor Ort; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

Excelya Group in Paris is seeking a Senior Clinical Project Manager to oversee international pediatric oncology trials. You will coordinate cross-functional teams, manage study timelines, budgets, and quality objectives, and ensure compliance with ICH-GCP and regulatory requirements.

You will drive recruitment, vendor relationships, risk mitigation, and study governance, contributing to innovative research with global impact in a collaborative 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

Communication skills

Stakeholder management

Leadership

English fluency

Ausbildung

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

Jobbeschreibung

Excelya Group in Paris is seeking a Senior Clinical Project Manager to oversee international pediatric oncology trials. You will coordinate cross-functional teams, manage study timelines, budgets, and quality objectives, and ensure compliance with ICH-GCP and regulatory requirements.

You will drive recruitment, vendor relationships, risk mitigation, and study governance, contributing to innovative research with global impact in a collaborative environment.