Clinical Trial Manager

Join ICON plc as a Clinical Trial Manager (CTM) in Paris/Ile-de-France!

ICON plc is a world leader in healthcare intelligence and clinical research. From molecule to medicine, we provide outsourced services to pharmaceutical, biotechnology, medical device, and public health organizations. With a patient-centered focus, we accelerate the development of life-saving drugs and devices that improve quality of life.

Our people are our greatest strength and the driving force behind our success. ICON people are passionate about achieving success and ensuring excellence in everything we do.

We are looking for motivated, reliable, and dedicated Clinical Trial Managers (CTMs) in the Paris/Ile-de-France area to join our sponsor-dedicated team!

What You Will Bring:

You will demonstrate prior experience as a Clinical Trial Manager, Local Trial Manager, or Study Manager in the pharmaceutical industry or a CRO.

Work format: Hybrid model with 1-3 days/week at the client office.

Your Role:

In this role, you will be the primary point of contact for leading, managing, and coordinating the execution of clinical trials from study start-up to close-out at the country level in France. You will ensure the quality and scientific integrity of clinical trials, collaborating with cross-functional stakeholders to ensure timely and on-budget delivery of clinical trial milestones within France.

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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