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Advanced Monitoring & CRA Skills

This practical course will introduce experienced monitors and CRAs to the more complex aspects of clinical trial monitoring and prepare them to work at a more senior level. This topic covers advanced study site management and monitoring of clinical trials. Topics include how to plan monitoring visits more effectively and proactively, how to use the criteria matrix to select the most appropriate investigators, monitoring various data collection methods (eg e-source). It also focuses on co-monitoring, dealing with difficult sites and how to motivate staff, problem solving, working under tight timelines, detecting fraudulent data, patient recruitment and retention issues, and appropriately documenting and reporting issues. This course will take you through these important areas of advanced monitoring to help ensure that you will be effective and meet the more stringent GCP inspection requirements that we now have in Europe.

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About Us

Since 1987, we have been delivering quality training to the pharmaceutical, healthcare, CRO and related industries. As well as delivering technical courses supporting clinical research functions, we also offer a wide range of personal development courses to ensure that skills learnt can be applied in the workplace.

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Rostrum Training Solutions Ltd

24 Lansdowne Road
RG30 4QU

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