Clinical Trial Manager: Lead Global Trials & Compliance

ICON Clinical Research; Paris; Sur place; EUR 70 000 - 100 000; Plein temps

Avantages offerts par ce poste

Annual leave

Health insurance

Retirement planning

EAP LifeWorks

Life assurance

Flexible benefits

Résumé du poste

ICON Strategic Solutions in Paris is seeking a Clinical Trial Manager to lead day-to-day trial operations across our clinical programmes. You will plan and manage trials, collaborate with cross-functional teams to implement protocols, and build strong investigator relationships to deliver high-quality outcomes.

The role requires solid trial management experience, regulatory know-how, and willingness to travel up to 25%.

Qualifications

• University degree in medicine, science, or equivalent combination of education & experience
• Demonstrated ability to drive the clinical deliverables of a study
• Subject matter expertise in the designated therapeutic area
• Willingness to travel approximately 25%

Responsabilités

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Connaissances

Clinical trial management

Stakeholder management

Regulatory compliance

Team development

Travel willingness

Formation

University degree in medicine/science

Description du poste

ICON Strategic Solutions in Paris is seeking a Clinical Trial Manager to lead day-to-day trial operations across our clinical programmes. You will plan and manage trials, collaborate with cross-functional teams to implement protocols, and build strong investigator relationships to deliver high-quality outcomes.

The role requires solid trial management experience, regulatory know-how, and willingness to travel up to 25%.