Clinical Trial Project Manager

☞ icometrix

Vue: 155

Jour de mise à jour: 26-11-2025

Localisation: Leuven Flemish Brabant

Catégorie: Planification / Projets

Industrie: Hospitals Health Care

Niveau: Entry level

Type d’emploi: Full-time

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le contenu du travail

We currently are looking for a project manager (with a first experience) to join our operational team in Belgium. Are you looking forward to managing a wide variety of global, multi-center clinical trials and research projects?

What will you do?
 icometrix acts as a specialised imaging CRO in the field of neurology. We use regulatory cleared software to perform image quantification in combination with radiological reading to evaluate drug efficacy and safety in phase I-IV clinical trials and real world studies.

You will be a project manager for such a clinical trial, managing the study end-to-end, including site onboarding and training, sponsor communication, data management, trial documentation and image analyses. You ensure that milestones, deliverables, timelines, budget, and quality of such trials, as outlined by the study protocol, monitoring plan, SOPs, and applicable regulations and policies are met. You are part of a team of project managers that support each other and communicate with sales, product and IT teams to guarantee optimal project alignment.

This means that you:
  • Oversee, report and present study status, timelines, budget and quality of team deliverables to the Project Team and Management.
  • Coordinate Neuro Imaging services and assure quality and clarity of clinical results for the correct interpretation by radiologists, neurologists, or other physicians.
  • Are accountable for the start-up activities ensuring that allocated trials are started within the defined timelines and accountable for Supervision of the ongoing Imaging part of a clinical trial.
  • Lead study-specific decision-making, develop strategies for increasing study efficiencies and co-ordinate issue detection and resolution.
  • Monitor progress and compliance of all aspects of the study plan and monitoring plan, with attention to Data management, Risk assessment and execution, contribution for submission ethics committees.
  • Identify risks and issues and escalate to the Team Manager; you provide corrections when needed.
  • Prepare meetings and interact with vendors and other stakeholders, if required.
  • Prepare and support potential audits and inspections.
  • Have a critical view on the study results and report proactively to the Team Manager on all study-related issue.
  • Participate in the development and coaching of less experienced staff.

What do we think you need?
  • Fit with our values and culture.
  • A first experience related to Clinical Trials Project Manager or Previous CRA experience.
  • A basic understanding of neuroimaging modalities, and in particular magnetic resonance imaging and quantification.
  • A basic understanding of neurology, and in particular Multiple Sclerosis.
  • Master’s degree or equivalent through working experience, master’s degree related to neuroimaging or neuroscience is a plus.
  • Clinical research or project management certifications are a plus.
  • Good stakeholder management and communication skills.
  • Eager to learn with positive energy and a results-oriented attitude.
  • Entrepreneurial, multicultural experience, customer-oriented.
  • Use problem-solving skills and appropriate resources to deal with requests and problems.
  • Work accurately and independently as well as within a multidisciplinary team.

What do we offer you?
  • A market conform wage.
  • A job advancing healthcare and technology.
  • A chance to work with experts in different areas and exchange ideas.
  • A dynamic, growing company with a worldwide impact.
  • An opportunity to have a direct impact on our product.
  • An innovating and challenging environment.
  • Enthusiastic and helpful colleagues.

Interested?
 Apply now via the application button.

Agency calls are not appreciated.
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Date limite: 10-01-2026

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