Clinical Scientist

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.

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

Missions :

• Support and represent the Study Medical Manager in all oncology study-related activities from setup to closure.
• Contribute to the elaboration of trial-related documents: abbreviated protocol, protocol, informed consent (ICF), protocol and ICF amendments, medical data validation plans, responses to medical questions, and participation in various meetings (investigators, monitors, etc.), including study committees’ preparation.
• Perform medical review of data on patient profiles, listings, and CIOMs.
• Collaborate closely with Trial Operations (TO), Pharmacovigilance (CME / GSO), and Statistics for establishing listings necessary for data review and consistency checks.
• Review study-related documents: CRF, CRF completion instructions, deviations list, validation plan, protocol review form, etc.
• Assist in reviewing interim and final study reports, associated statistical tables, and draft publications.
• Conduct medical review of files, listings, and contribute to clinical study management (protocol writing, basic clinical analysis, study setup, medical training, medical responses) in oncology studies, regardless of study type.
• Write medical review guidelines for outsourcing or applicable contexts.

About You

At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values.

• Experience: Proven ability to thrive in collaborative, fast-paced environments; talent matters most—no minimum years required.
• Skills: Strong organizational abilities, problem-solving mindset, and excellent communication skills.
• Education: Knowledge in immunology is recommended.
• Languages: Fluency in French and a good level of English.