Clinical Trial Manager – Belgium (Leuven) – Infectious Disease / Immunology

Overview

In this role you will oversee day-to-day operations of clinical studies in Leuven, Belgium, applying ICH/GCP standards within a CRO context. You will serve as the main sponsor contact for operational issues and study deliverables, while maintaining deep knowledge of protocols, therapeutic areas, and indications. You will coordinate a cross-functional project team, ensure training, and drive risk management and vendor oversight. This is a growth-focused opportunity in immunology and infectious diseases, with remote flexibility after probation and a competitive compensation package.

Pay / Benefits

• flexible work environment
• competitive compensation and benefits package
• competitive PTO
• structured career paths
• employee appreciation events
• employee health and wellness initiatives

Responsibilities

• Oversee day-to-day project operations per contract and regulatory requirements
• Act as primary sponsor contact for operational issues and study deliverables
• Maintain protocol and therapeutic area knowledge to guide study execution
• Provide cross-functional oversight and ensure necessary project training
• Review and input on study protocol, edit check specs, data analysis plan, and final report when applicable
• Develop operational project plans and manage risk assessment and execution
• Oversee vendor management for studies
• Ensure site quality and supervise CRAs and monitoring deliverables

Key requirements

• Bachelor in Health or Life Science; advanced degree preferred
• Phases 1-4 experience, with Phases 2-3 preferred
• Minimum 2 years of Clinical Trial Management experience; CRO experience preferred
• Experience managing overall project timelines
• Bid defense experience preferred
• Strong leadership skills

• strong leadership
• stakeholder management
• effective communication
• ICH/GCP knowledge
• protocol and data analysis plan review
• vendor management

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