Clinical Team Lead - Sponsor dedicated

Fortrea; Paris; Sur place; EUR 90 000 - 130 000; Plein temps

Résumé du poste

Fortrea seeks a Clinical Team Lead (Local Trial Manager) in France. This full-time role is dedicated to a single sponsor with responsibilities spanning end-to-end operational oversight, CRO/vendor management, and site performance, ensuring timely data delivery and quality.

The position emphasizes RBQM-aligned risk management and inspection readiness. Qualified candidates will have a life sciences degree and solid clinical research experience in pharma or CRO settings, including trial management

Qualifications

• University/college degree in life sciences or related field.
• Experience in clinical research within pharma or CRO.
• Experience in trial management preferred.
• Knowledge of local regulatory environment.
• Understanding of trial planning, management, and metrics.

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 issues.
• Monitor progress, timelines, and quality metrics; implement mitigation plans.
• Drive risk identification and resolution in line with RBQM principles.
• Ensure inspection-readiness through TMF, monitoring reports, and issue management.
• Partner with data management, medical, and safety teams for timely data delivery.

Connaissances

Clinical trial management

Regulatory knowledge

Cross-functional leadership

Communication skills

Formation

Life sciences degree

Description du poste

We are looking to hire a Clinical Team Lead (Local Trial Manager) in France. In this position, you will be fully dedicated to a single sponsor. This position is open for full-time candidates.

Responsibilities

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

Education, Skills And Other Requirements

• University/college degree (life science preferred), or certification in a related allied health profession
• Previous experience in clinical research in pharmaceutical or CRO industries
• Previous experience in managing trials preferred
• Deep understanding of local regulatory environment
• Strong understanding of clinical trial planning, management and metrics is important as well as the ability to focus on multiple deliverables and protocols at a time

Experience (Minimum Required)

• Minimum of three (3) years of relevant clinical research experience in a pharmaceutical company/CRO.
• In lieu of the above requirements, candidates with greater than four (4) years supervisory experience in a health care setting of which two (2) years clinical research experience (including monitoring) in the pharmaceutical or CRO industries will be considered.
• Ability to work with minimal supervision.
• Excellent verbal and written communication skills.
• Ability to set clear expectations for junior staff on projects.
• Ability to resolve project-related problems and prioritizes workload for self and team.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com. Learn more about our EEO & Accommodations request here.