8 meilleures offres (clinical research, bruxelles capitale) (à pourvoir)

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(Associate) Medical Director - Neurology
Thermo Fisher Scientific —Bruxelles
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Clinical Trial Operations Specialist

Excelya -
Bruxelles

Postuler rapidement

Détails de l'emploi

Temps plein
Il y a 10 heures

Qualifications

Français
Anglais
Recherche
Master
Bachelier

Description complète du poste

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 combines operational excellence, clinical trial coordination, and regulatory compliance, playing a key role in ensuring the seamless execution of clinical studies across a global environment. Ideal for a highly organized professional passionate about clinical operations, stakeholder collaboration, and delivering high-quality trial support.

Main Responsibilities:

Coordinate and support the planning, execution, and reporting of clinical trials at site and country level.
Ensure timely preparation, collection, and maintenance of trial documentation and regulatory records.
Maintain oversight trackers and trial management systems to support study execution and reporting.
Support Trial Master File (TMF) quality, completeness, and compliance with applicable regulations.
Coordinate local study activities, meetings, and communication with internal and external stakeholders.
Facilitate collaboration between clinical teams, investigational sites, and vendors.
Manage and track study-related supplies and operational requirements at site level.
Ensure the accurate set-up, maintenance, and administration of clinical trial systems and user access.
Monitor data quality, consistency, and completeness across trial management tools.
Support compliance with ICH-GCP, Good Documentation Practice, SOPs, and local regulatory requirements.

Requirements

Master or Bachelor degree in Life Sciences, Administration or related field
Previous experience in clinical research, clinical operations, clinical trial administration in a CRO environment
Good understanding of ICH-GCP principles and Good Documentation Practices.
Understanding of Trial Master File (TMF) processes and clinical trial documentation requirements.
Fluent in English and French or Dutch
Ability to work autonomously, manage multiple priorities, and collaborate effectively in a matrix environment
Strong teamwork and stakeholder management skills.

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.

Postuler rapidement

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clinical research emplois - bruxelles capitale

Clinical Trial Operations Specialist

Medical Development Program - Physician (New to Industry)

Clinical Research Associate - French Speaking - Any EMEA location

Clinical Trial Supply Manager – Brussels, Belgium (F/M)

Data Science Lead

Medicine Specialist (Fluent in French) - Freelance AI Trainer Project

Medical Advisor Opthalmology /New Products (M/F/D)

(Associate) Medical Director - Neurology

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : clinical research (bruxelles capitale)

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