Clinical Research Associate

il y a 2 semaines

Paris, France Excelya Temps plein

**About the Job**

Join Excelya, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main responsibilities:

- Ensure the proper conduct of clinical trials in oncology from initiation to close-out
- Select investigator sites, set up studies, and monitor clinical trial progress
- Manage and track clinical trial budgets
- Handle required administrative tasks for study start-up and ongoing operations
- Conduct monitoring and co-monitoring visits at investigator sites
- Maintain regular communication with investigators and site staff
- Review clinical trial instructions and documentation as needed
- Prepare sites for audits and inspections, and actively participate in these processes
- Document and track any deviations or issues observed during the study

**Requirements**:
**Experience**:Prior experience or knowledge in **oncology clinical trials** is essential.

**Skills**:Solid knowledge of the full monitoring lifecycle for clinical trials (site selection, initiation, inclusion, follow-up, and closure). Familiarity with clinical research phases I, II, and III.

**Education**:Bachelor's degree in a life science or related discipline (or equivalent qualification).

**Languages**:Fluent in French and in English.

**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.

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