Central Monitoring Manager

☞ EASYRECRUE

Ver: 140

Día de actualización: 16-11-2025

Ubicación: Leuven Flemish Brabant

Categoría: Gerencia ejecutiva

Industria:

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Contenido de trabajo

With the industry moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would set the grounds for risk-based models on the clinical study level, mitigate data quality issues, and streamline monitoring, while ensuring patient safety and valid study results.

Office-Based in Leuven, Belgium

You will

  • Facilitate risk assessment, identify issues & critical data before and during study conduct
  • Develop and review study-specific Monitoring Plans
  • Select and setup RBM system; deliver relevant training to project teams
  • Monitor aggregated patient and site data using technology
  • Conduct root cause analysis of risks during study conduct
  • Support Project Managers and Site Monitors in optimizing source data verification and site visit schedules
  • Maintain documentation of central monitoring activities
  • Contribute to Proposals and bid defense meetings with information about Central Monitoring services

Qualifications

  • College/University degree or an equivalent combination of education, training and experience
  • Experience in central monitoring in clinical trials
  • Knowledge of clinical trial process, ability to understand the protocol and study associated risks
  • Critical thinking and analytical skills
  • Ability to work with complex data and provide insight into risk reports and trends
  • Communication skills, ability to explain complex concepts
  • Full working proficiency in English
  • Proficiency with MS Office applications, advanced Excel skills
  • Knowledge of basic statistical concepts

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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Plazo: 31-12-2025

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