Clinical Trial Manager

We are constantly looking for motivated, reliable and dedicated CTMs who can demonstrate a first similar experience as a Clinical Trial Manager, Local Trial Manager or Study Manager within the pharmaceutical industry or a CRO.

As a Clinical Trial Manager you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.

We are currently looking for a Clinical Trial Manager based in Paris (home based).

In this role you will be a primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out at a country level in France. You will maintain the quality and scientific integrity of clinical trials at a country level. Local Trial Manager collaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables within the country.

Key responsibilities include: 

• Planning, management and oversight of clinical study execution in accordance with the global program strategy
• Accountable for study deliverables in France
• Lead country-level operational planning and support site selection within assigned country
• Ensure key stakeholders are kept informed of study progress
• Communicate country status (including timelines and deliverables) to key stakeholders and ensure updates to relevant systems
• Oversight and monitoring of applicable vendor activities eg. laboratories and equipment provisioning
• Monitor the execution of the clinical study against timelines, deliverables and budget for France
• Review Monitoring Visit Reports
• Contribute to the study-level forecast for investigational product, support study level accountability and reconciliation, management of ELE process
• Execute regulatory agency inspection readiness activities
• Assign and oversee deliverables of study support staff
• Collaborate with local teams to ensure country level study delivery is aligned with global expectations

You will need:

• A first stable experience as a CTM, this within the pharmaceutical industry or a CRO (min 2 years)
• Prior monitoring experience
• Excellent organization skills
• Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
• Strong IT skills
• Strong communication with the ability to multitask and work effectively under pressure
• Fluency in French and professional proficiency in English

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