Senior Project Coordinator

Triwill Group; France; Sur place; EUR 60 000 - 90 000; Plein temps

Résumé du poste

Triwill Group is representing a partner company seeking a Senior Project Coordinator based in France to support site activation and deliverables across the clinical trial lifecycle. You will work with Project Managers, CTMs, Site Selection teams, CRAs, and clinical sites to ensure timelines and quality are maintained while mentoring junior colleagues.

The role involves autonomous work in a fast-growing clinical research environment and contributes to successful trial delivery.

Qualifications

• Senior Project Coordinator with responsibilities across clinical trial lifecycle.

Responsabilités

• Support site activation and site-level deliverables throughout the clinical trial lifecycle.
• Collaborate with Project Managers, Clinical Trial Managers, Site Selection teams, CRAs, clinical sites and other stakeholders.
• Own timelines, quality and priorities to help ensure sites are activated efficiently and trials stay on track.
• Mentor junior colleagues when needed.

Description du poste

Description:

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Project Coordinator based in France.

As a Senior Project Coordinator, you will play a key role in supporting site activation and site-level deliverables throughout the clinical trial lifecycle. You will collaborate closely with Project Managers, Clinical Trial Managers, Site Selection teams, CRAs, clinical sites, and other stakeholders. The role combines project coordination, regulatory documentation, communication, and operational oversight in a global, multi-regional environment. You will take ownership of timelines, quality, and priorities to help ensure sites are activated efficiently and trials remain on track. As a senior team member, you will work autonomously while also supporting and mentoring junior colleagues when needed. This is an opportunity to make a tangible impact in a fast-growing clinical research environment while contributing to the successful delivery of clinical trials.