Advanced Monitoring In Clinical Trials-Corporate

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An interactive and comprehensive course that encompasses all the aspects of clinical trials monitoring, from regulatory requirements to monitoring oversight, for all phases of a clinical trial study.

This course covers advanced and complex topics of clinical trials monitoring, and prepares experienced monitors to further expand their skills and knowledge to function at a more senior level.

 

THE PROGRAM

This course covers the advanced aspects of site management, monitoring skills and monitoring oversight. This is an interactive and comprehensive course that encompasses advanced techniques and principles in clinical trials monitoring, with reference to regulatory requirement for all phases of a clinical trial study.

The course will cover topics in sites selection, improvement in subject recruitment and retention, and issues relating to informed consent, source data verification, deviations, electronic data management, documents management, as well as communication skills in dealing with pharmacists, laboratories and ethics committee.

Note:This program is designed for professionals with at least two years of experience in the clinical research industry.

 

COURSE OBJECTIVE

  • Understand current thinking on risk based monitoring approaches and develop appropriate monitoring strategies for your study
  • Develop superior strategies for selecting sites, recruiting patients and motivating investigational sites
  • Significantly improve your performance as a monitor to an advanced level
  • Use effective planning and tracking tools to maximise efficiency as a monitor
  • Develop strategies for dealing with complex monitoring issues
  • Gain expertise in monitoring oversight activities

 

WHO SHOULD JOIN

  • Clinical Research professionals and associates
  • Clinical Scientist / Basic Scientist
  • Clinical Investigators / Principal Investigators
  • Experienced Clinical Quality Assurance Professionals
  • Project Managers
  • Clinical Study Coordinators
  • GCP-focused Regulatory Affairs Professionals
  • Professionals that had undergone basic monitoring training