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Subject Recruitment in clinical trials is by far the greatest cause of delays in clinical trials. Some of the delays can be significant and affect the entire clinical development plan of a product.





This is an interactive and comprehensive course emcompassing all aspects of subject recruitment and retention in clinical trials and how this should be managed effectively from managing expectations of the Sponsor and Sites to bring targets back on track should things not go to plan.

Topics include risk assessment and minimization for subject recruitment and retention, feasibility and recruitment plans, methods of recruitment and how these can be adapted for different therapeutic areas, tracking and escalation of recruitment and retention and strategies that can be used to bring recruitment and retention back on track. The workshop is designed to maximize learning by presenting a mixture of theory and then application of the theory through fun group exercises and games.



  • Understand the impact of subject recruitment on the clinical development plan of a product
  • Appreciate the impact that subject retention has on the results of the study
  • Develop superior strategies for assessing investigational sites and setting expectations for recruiting and retaining patients
  • Gain insight into a wide range of effective methods of recruitment for different therapeutic areas and settings
  • Use effective planning and tracking tools to maximise efficiency of subject recruitment and retention
  • Develop strategies for bringing recruitment back on track



  • Clinical Research professionals and associates
  • Clinical Scientist / Basic Scientist
  • Clinical Investigators / Principal Investigators
  • Experienced Clinical Quality Assurance Professionals
  • Project Managers
  • Clinical Study Coordinators
  • Professionals in Clinical trials


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