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Excelya recrutement

Clinical Research Associate H/F Excelya

  • Dijon - 21
  • CDI
  • Bac +5
  • Industrie Pharmaceutique • Biotechn. • Chimie

Les missions du poste

About the Job

Join Excelya, whereAudacity, Care, and Energydefine 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 :

- 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

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.

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.

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.

Localiser le poste

Publiée le 12/09/2025 - Réf : bf36c303-8f47-4140-94cd-bdb6de40ed88

Clinical Research Associate H/F

Excelya
  • Dijon - 21
  • CDI
Publiée le 12/09/2025 - Réf : bf36c303-8f47-4140-94cd-bdb6de40ed88

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