France Clinical Team Lead — Local Trial Manager (FT)

Fortrea; Paris; Sur place; EUR 75 000 - 110 000; Plein temps

Résumé du poste

Fortrea is seeking a Clinical Team Lead (Local Trial Manager) in France. This role is fully dedicated to a single sponsor and available to full-time candidates.

You will oversee end-to-end trial operations, lead cross-functional teams, monitor progress and quality metrics, and drive risk mitigation in collaboration with data management, medical, and safety groups. The position requires strong regulatory knowledge and leadership capabilities.

Qualifications

• Must have clinical research experience in pharmaceutical or CRO settings.
• Strong understanding of local regulatory frameworks governing trials.
• Proven leadership and ability to manage cross-functional teams.
• Excellent verbal and written communication skills are essential.
• Ability to manage multiple deliverables and timelines simultaneously.

Responsabilités

• Provide end-to-end operational oversight for assigned studies, including CRO/vendor and site performance.
• Lead cross-functional study team meetings and act as escalation point for site-level issues.
• Monitor study progress, timelines, and quality metrics; implement mitigation plans.
• Drive proactive risk identification and resolution aligned with RBQM principles.
• Ensure inspection readiness through TMF oversight, monitoring reports, and issue management.
• Partner with data management, medical, and safety teams to ensure timely data delivery.

Connaissances

Clinical research

Regulatory knowledge

People leadership

Communication skills

Project management

Formation

Life science degree

Clinical research certification

Description du poste

Fortrea is seeking a Clinical Team Lead (Local Trial Manager) in France. This role is fully dedicated to a single sponsor and available to full-time candidates.

You will oversee end-to-end trial operations, lead cross-functional teams, monitor progress and quality metrics, and drive risk mitigation in collaboration with data management, medical, and safety groups. The position requires strong regulatory knowledge and leadership capabilities.