Description
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.