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Clinical Scientist I&I

Excelya

Gentilly, Île-de-France, France Hybrid permanent

Posted: February 11, 2026

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Quick Summary

A Clinical Scientist I&I is responsible for collaborating with a multidisciplinary team to drive the success of clinical trials in immunology and inflammation, delivering innovative research and contributing to the development of new treatments.

Job Description

About the Job

At Excelya, we embrace our core values of Audacity, Care, and Energy to shape the future of clinical research. As a Clinical Scientist in Immunology & Inflammation (I&I), you will collaborate closely with a talented multidisciplinary team to drive the success of our clinical trials.

This position provides an opportunity to engage in innovative research and contribute to studies aimed at addressing critical medical needs. You will be integral to ensuring the smooth execution of clinical trials while maintaining the highest scientific and ethical standards.

• Support and represent the Study Medical Manager throughout all clinical study activities, from study set-up to closure
• Contribute to the development and review of clinical trial documentation (protocols, amendments, informed consent forms, medical data validation plans) in Immunology & Inflammation clinical development
• Draft responses to medical queries from health authorities, ethics committees, clinical sites, and internal stakeholders, and contribute to study-related meetings
• Assist in the preparation and management of study committees, including member coordination, charter development, meeting organization, reporting, and documentation
• Maintain and manage medical and scientific documentation within the Trial Master File (TMF)
• Perform clinical case reviews, including patient profile assessment and validation of clinical narratives
• Collaborate closely with Trial Operations, pharmacovigilance, and biostatistics teams to support data review and reporting activities
• Review study-related documents (risk management plans, CRF and completion guidelines, monitoring plans, deviation lists, etc.)
• Contribute to interim and final study reports, CSR appendices, statistical outputs, and draft publications
• Support data review processes, statistical surveillance, medical validation, and overall clinical study management activities
• Develop medical review guidelines where applicable, including in outsourcing contexts
• Prepare documentation and support activities related to audits and inspections ensuring compliance and readiness.


Requirements:
About You

At Excelya, we foster an environment where audacious steps are encouraged. We seek innovative thinkers who are committed to excellence in clinical research.

• Experience: Experience in clinical research, particularly in immunology and inflammation areas is preferred but not strictly required—talent matters most to us!
• Skills: Ability to work effectively in a cross-functional team environment, with strong analytical, problem-solving, and communication skills. Familiarity with regulatory standards and GCP.
• Education: PharmD, PhD, or Master's degree in Life Sciences, with a focus on Immunology, Biology, or a related scientific discipline.
• Languages: Fluency in English and in french.


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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