Clinical Operations Consultant

Jobtailor; Brussel Hoofdstad; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

Excelya, based in Brussels, is seeking a professional to drive innovation and impact in clinical research. This role involves supporting the operational management of ongoing clinical studies and collaborating with internal and external stakeholders.

The successful candidate will have solid experience in Clinical Operations, strong stakeholder management abilities, and fluency in English. Join our ambitious team to redefine excellence in healthcare and enhance the patient journey.

Qualifications

• Solid experience in Clinical Operations within clinical research.
• Strong understanding of clinical trial execution from the CRO perspective.
• Experience with sponsor-side oversight activities is highly preferred.

Responsabilités

• Support the operational management of ongoing clinical studies.
• Contribute to study oversight and coordination activities.
• Collaborate with internal and external stakeholders.

Connaissances

Clinical Operations experience

Stakeholder management

Communication skills

Fluency in English

Description du poste

JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.

This roleisanexcitingopportunitytocontributetoadynamic,ambitiousteam.Youwillplayacriticalpartindrivinginnovationandmakinganimpactintheclinicalresearchspace,whileenjoyingastimulatingprofessionalenvironmentthatencouragespersonalandintellectualgrowth.

Main Responsibilities

• Support the operational management of ongoing clinical studies.
• Contribute to study oversight and coordination activities.
• Collaborate with internal and external stakeholders, including CRO partners and study teams.
• Ensure compliance with applicable regulations, GCP and study procedures.
• Assist with workload management and operational delivery during a peak activity period.

Requirements

• Solid experience in Clinical Operations within clinical research.
• Strong understanding of clinical trial execution from the CRO perspective.
• Experience with sponsor-side oversight activities is highly preferred.
• Ability to work independently and support ongoing study activities in a fastpaced environment.
• Strong stakeholder management and communication skills.
• Fluent in English; additional local languages are a plus.

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'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.