Les missions du poste
About the Job
Join Excelya, a company driven by Audacity, Care, and Energy, where innovation and collaboration are at the heart of everything we do. As a Clinical Scientist, you will be a key player in supporting clinical trials and contributing to the advancement of clinical research projects.
You will work alongside cross-functional teams to ensure clinical studies are conducted in accordance with protocol, regulatory requirements, and company standards. Your role will involve reviewing clinical data, supporting medical monitoring activities, and contributing to the development and review of clinical trial documents.
- Support clinical trial activities from study start-up to close-out, ensuring adherence to clinical and regulatory standards.
- Contribute to the preparation and review of protocols, informed consent forms, and amendments.
- Perform medical review of clinical data, including patient profiles and adverse event narratives.
- Collaborate with pharmacovigilance, clinical operations, and biostatistics teams for data review and interpretation.
- Assist in medical writing and review of study-related documents such as clinical study reports and briefing documents.
- Ensure proper documentation and filing of study-related materials into Trial Master Files.
- Support preparation for audits, inspections, and regulatory submissions.
Le profil recherché
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'sleading mid-size CROwith thebest employee experience. Ourone-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 caremeans 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 You
At Excelya, we value talent and a proactive mindset over rigid experience requirements. We seek passionate individuals who align with our core values.
- Experience: Experience in clinical research or related fields is beneficial but we prioritize your skills and motivation.
- Skills: Strong analytical and clinical data review skills, ability to collaborate in cross-functional teams, familiarity with GCP and clinical trial regulations.
- Education: Advanced degree in Life Sciences such as PharmD, MD, PhD, or MSc in Biology or related fields.
- Languages: Proficiency in English; knowledge of French is a plus.
Bienvenue chez Excelya
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.
Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.
We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.
Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.
Publiée le 08/06/2026 - Réf : 15fc99fa-7ba0-43d4-b19c-08121b779d26
