Risk Management in Clinical Research

 

Risk Management in Clinical Research

Clinical Operations Courses

You want to know the ins and outs of risk management in clinical research? You want to be prepared and try to avoid problems in your trials? Follow this course with a focus on risk monitoring and risk management techniques.

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850,00 €
  • Full description & trainer
  • Programme highlights
  • Learning objectives
  • Workshops & extras
Full description

This is a one day course introducing the ins and outs of risk management in clinical research (not to be confused with risk management in pharmacovigilance). It demonstrates the importance of using risk monitoring and risk management techniques in Clinical Research Programme Management. Participants will learn how to define, evaluate and characterise risks and also how to devise and implement specific techniques and strategies for risk management. This course is divided into three interactive workshops. The course concludes with a lively discussion and action planning session with all participants.

Who should attend?

Clinical Research Managers and Project Managers. Lead Clinical Research Associates (CRAs) who want to set new goals for their career as clinical
research project team leaders.

Trainers
  • To identify risks associated with clinical projects
  • To learn how to assess risks & avoid risk areas
  • To evaluate the risk benefits and prioritize
  • To reduce impact on other projects and the likelihood of failure
  • To develop risk-handling strategies and management plans
Workshops
  • Workshop Risk Identification: Defining specific risks associated with clinical research - Benefits of risk management techniques - Role of Project Managers
  • Workshop Risk Assessment: Draw risk management process - Evaluating and prioritizing risks
  • Workshop Risk Monitoring and Risk Management Plans: Developing risk handling strategies - Risk management: work-arounds & deficiencies