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Clinical Trial Assistant – France

TN France

France

Sur place

EUR 30 000 - 60 000

Plein temps

Il y a 17 jours

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Résumé du poste

An innovative health company is seeking a Clinical Trial Assistant to join their dynamic team in France. This exciting role involves managing various stages of clinical trials, from setup to closure, while ensuring compliance and quality control. You will collaborate with leading experts and contribute to impactful projects that enhance patient care. The company values audacity, care, and energy, fostering an inclusive environment that promotes personal and professional growth. If you're passionate about making a difference in clinical research, this opportunity is perfect for you.

Qualifications

  • Experience in clinical trial management and administrative tasks.
  • Strong communication skills and ability to work in teams.

Responsabilités

  • Manage administrative and budgetary activities for clinical trials.
  • Coordinate with CROs and vendors for smooth trial execution.

Connaissances

Project Management
Communication
Regulatory Compliance

Formation

Bachelor's Degree in Life Sciences
Master's Degree in Clinical Research

Outils

VeevaVault

Description du poste

Social network you want to login/join with:

Clinical Trial Assistant – France, france

Client:

Excelya

Location:

France

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

bc8c19bcfcb6

Job Views:

2

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

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

  • Administrative and budgetary activities for the various stages of a clinical trial (set-up, follow-up, and closure)
  • Participation in project team meetings
  • VeevaVault eTMF management: document loading and quality control of clinical trial documents
  • Support for site management activities, including communication with investigational sites and tracking essential documents
  • Coordination with CROs, vendors, and internal teams to ensure smooth trial execution
  • Assistance in regulatory submissions and compliance tracking
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