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Central Monitoring Manager

  • Location: Oxford
  • Salary: Competitive
  • Contract hours: FullTime

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About the job

Company Description

PSI is a leading Contract Research Organization with more than 22 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

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 Oxford

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

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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