Attaché de Recherche Clinique - Cancérologie Digestive

Excelya; Dijon; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading health company is seeking a Talent Acquisition Partner in Dijon, France. This role involves recruiting for clinical research profiles and requires knowledge of oncology clinical trials and monitoring lifecycle management. The ideal candidate should hold a Bachelor's degree in a relevant field and be fluent in French and English. Join a dynamic team that values innovation and personal growth.

Qualifications

• Prior experience or knowledge in oncology clinical trials.
• Solid knowledge of the full monitoring lifecycle for clinical trials.
• Fluent in French and in English.

Responsabilités

• Organize and conduct study initiation visits remotely for clinical trials.
• Support CRAs by managing study start-up set-up activities.
• Ensure proper implementation of study documentation during SIVs.
• Contribute to additional ad-hoc tasks related to clinical trial management.

Connaissances

Monitoring lifecycle knowledge

Oncology clinical trials experience

Bilingual in French and English

Formation

Bachelor's degree in life science or related field

Description du poste

Overview

Talent Acquisition Partner at Excelya | Recruiting Clinical Research Profiles

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.

Responsibilities

• Organize and conduct study initiation visits (SIVs) remotely via webinars for Phase II & III clinical trials
• Support other CRAs by managing study start-up set-up activities related to site initiation
• Ensure that all study documentation, training, and regulatory requirements are properly implemented during SIVs
• Contribute to additional ad-hoc tasks related to clinical trial management, if required

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 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.