Clinical Quality Assurance Specialist – France

Excelya; France; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Rejoignez Excelya en tant que Clinical Quality Assurance Specialist, où vous contribuerez à une équipe dynamique d'opérations cliniques. Cette opportunité vous permet de jouer un rôle clé dans l'innovation et l'impact de la recherche clinique tout en favorisant votre croissance personnelle et professionnelle.

Qualifications

• Expérience en gestion de la documentation ou en recherche clinique.
• Connaissance des procédures opérationnelles standard (SOP).
• Capacité à travailler en équipe et à résoudre des problèmes.

Responsabilités

• Rédiger et réviser les procédures opérationnelles standard (SOP).
• Surveiller et suivre la résolution des CAPA liées à des audits.
• Mettre en œuvre des plans d'action pour les problèmes de qualité identifiés.

Description du poste

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Clinical Quality Assurance Specialist – France

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Client:

Excelya

Location:

France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

5c996c1e3c49

Job Views:

5

Posted:

30.05.2025

Expiry Date:

14.07.2025

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Job Description:

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 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

Quality Documentation Management

Draft and review standard operating procedures (SOPs) and work instructions.

Develop and implement document templates.

Update and maintain quality-related documents.

Distribute procedures to relevant personnel via e-learning platforms.

Track and ensure completion of training on quality procedures.

Quality Control & CAPA Management

Monitor and follow up on the resolution of audit-related CAPAs.

Conduct quality checks on specific processes or activities.

Implement action plans to address identified quality issues.