Senior Clinical Project Manager: Lead Global Trials

Excelya; Paris; On-site; EUR 70,000 - 90,000; Full time

Job summary

Excelya is seeking an experienced Clinical Project Manager to oversee local trial activities in France. You will coordinate operational aspects of interventional studies, ensuring ICH-GCP compliance and seamless collaboration with investigators, CROs, vendors, and global teams.

You will lead study management from start-up to close-out, manage timelines, quality, and risk mitigation, and act as the primary interface with local stakeholders. Fluency in French and English is required.

Qualifications

• Experienced in Clinical Operations within pharma or CRO.
• Experience as Clinical Project Manager, Study Manager, or equivalent.
• Involvement in interventional trials (Phase II-IV preferred).
• Solid understanding of ICH‑GCP, regulatory environment, and local clinical practices.
• Experience collaborating with investigators, CROs, and cross‑functional teammates.
• Strong organizational, operational, and communication skills.
• Ability to manage several tasks simultaneously in a fast‑paced environment.
• Fluency in French and English (written & spoken).

Responsibilities

• Lead and coordinate clinical trial activities at the local level from start-up to close-out.
• Ensure local execution of global study plans in alignment with timelines and quality standards.
• Serve as the key point of contact for local investigational sites and regional stakeholders.
• Work closely with global study teams, medical affairs, regulatory affairs, and clinical operations.
• Track KPIs, patient recruitment, timelines, and operational deliverables.

Skills

Clinical Operations

Study Manager

Interventional Trials

ICH-GCP

French & English

Job description

Excelya is seeking an experienced Clinical Project Manager to oversee local trial activities in France. You will coordinate operational aspects of interventional studies, ensuring ICH-GCP compliance and seamless collaboration with investigators, CROs, vendors, and global teams.

You will lead study management from start-up to close-out, manage timelines, quality, and risk mitigation, and act as the primary interface with local stakeholders. Fluency in French and English is required.