Senior Clinical Project Manager: Lead Global Trials

Excelya; Paris; On-site; EUR 70,000 - 100,000; Full time

Job summary

Excelya is seeking an experienced Clinical Project Manager to oversee local clinical activities in a pharmaceutical environment. You will coordinate trial operations, ensure regulatory compliance, and serve as the main liaison between investigators, vendors, and global teams.

The role requires strong autonomy, rigorous execution, and excellent communication to navigate cross-functional settings. You will manage study start-up through close-out and contribute to ongoing data quality and

Qualifications

• Experience 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 research practices.
• Experience collaborating with investigators, CROs, and cross-functional teammates.
• Strong organizational, operational, and communication skills.
• 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.
• Ensure that clinical trial activities comply with local regulations, ICH-GCP, and internal SOPs.
• Coordinate local submissions to competent authorities and ethics committees when required.
• Monitor adherence to regulatory timelines and manage any corrective actions.
• Support site selection, activation, monitoring, and close-out in collaboration with CRAs and vendors.
• Manage relationships with local vendors (logistics, labs, CRO partners).
• Follow up on recruitment progress, performance, and site-level metrics.
• Work closely with global study teams, medical affairs, regulatory affairs, and clinical operations.
• Participate in study meetings and provide updates on local activities, challenges, and achievements.
• Support risk mitigation plans and operational troubleshooting.
• Oversee data accuracy, query resolution, and compliance of documentation.
• Track KPIs, patient recruitment, timelines, and operational deliverables.
• Contribute to audit and inspection readiness.

Skills

Clinical Operations

Project Management

Interventional Trials

ICH-GCP

Stakeholder Collaboration

Bilingual FR/EN

Job description

Excelya is seeking an experienced Clinical Project Manager to oversee local clinical activities in a pharmaceutical environment. You will coordinate trial operations, ensure regulatory compliance, and serve as the main liaison between investigators, vendors, and global teams.

The role requires strong autonomy, rigorous execution, and excellent communication to navigate cross-functional settings. You will manage study start-up through close-out and contribute to ongoing data quality and