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

ICON plc is a global 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 approach, we accelerate the development of life-saving drugs and devices that improve quality of life.

Our people are at the heart of our success. ICON team members are passionate, driven, and committed to achieving excellence in everything we do.

We are currently 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:

• Minimum 2 years of experience as a Local Trial Manager (LTM) in a CRO.
• Living in Paris area and agree to visit the Sponsor's office for study meetings, team meetings, etc. (around once a month).
• Therapeutic area: Oncology/Onco-Hematology.
• 1-2 days at the client office during onboarding.

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 the 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.