Clinical Trial Manager

Key Responsibilities:

• Plan, manage, and oversee clinical study execution in alignment with the global program strategy.
• Take accountability for study deliverables in France.
• Lead country-level operational planning and support site selection within France.
• Ensure key stakeholders are informed of study progress, timelines, and deliverables.
• Communicate country status (including timelines and deliverables) to stakeholders and update relevant systems.
• Oversee and monitor the activities of external vendors (e.g., laboratories, equipment provisioning).
• Monitor study execution against timelines, deliverables, and budget in France.
• Review Monitoring Visit Reports and contribute to study-level forecasts for investigational products.
• Manage regulatory agency inspection readiness activities.
• Assign and oversee deliverables for study support staff.
• Ensure country-level study delivery aligns with global expectations.

What You Will Need:

• Previous experience as a CTM, Local Trial Manager or similar role within the pharmaceutical industry or CRO.
• Prior monitoring experience.
• Strong organizational skills and the ability to manage multiple priorities.
• Ability to work in a dynamic environment and adapt to changing business needs.
• Strong IT skills and the ability to multitask effectively under pressure.
• Fluency in French and professional proficiency in English.

If you're ready to take on an exciting challenge with a global leader, apply now and join our team at ICON!

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