Clinical Operations Consultant

Role Overview

• Support the operational management of ongoing clinical studies.
• Contribute to study oversight and coordination activities.
• Collaborate with internal and external stakeholders, including CRO partners and study teams.
• Ensure compliance with applicable regulations, GCP and study procedures.
• Assist with workload management and operational delivery during a peak activity period.

Requirements

• Solid experience in Clinical Operations within clinical research.
• Strong understanding of clinical trial execution from the CRO perspective.
• Experience with sponsor-side oversight activities is highly preferred.
• Ability to work independently and support ongoing study activities in a fastpaced environment.
• Strong stakeholder management and communication skills.
• Fluent in English; additional local languages are a plus.

Tech Stack

• Google Cloud Platform

Benefits

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here's what makes us unique !

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe's **leading mid-size CRO **with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.