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September 13-15, 2016
Boston, MA
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September 14-15, 2016
Boston, MA
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San Diego, CA
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September 6-8, 2016
San Francisco, CA







Subject Recruitment for Clinical Research Sites December 2010

Dec 15, 2010
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Course Description 

This course presents an overview of the patient recruitment arena today, and focuses on strategies for successful clinical trials including systematic protocol feasibility, pre-screening approaches, and in-sourcing and outsourcing options. Included in the program are discussions for handling tough populations and the ethics of participant recruitment in clinical trials.

VideoPreview 

 

Learning Objectives 

  • Explore updates on clinical trial participant recruitment worldwide
  • Discuss an overview of participant recruitment practices
  • Examine keys to success: systematic practice approaches to recruitment in clinical trials
  • Employ pre-screen practices to improve screening successes
  • Examine the consenting process in regard to subject recruitment and retention
  • Retain quality subjects to support data integrity
  • Implement strategies for managing susceptible populations
  • Evaluate efforts: the recruitment report card

Who Should Attend 

  • Clinical Research Coordinators
  • Site Research Managers
  • Clinical Research Monitors
  • Sponsor Project Managers

Instructor 

Sandra "SAM" Sather, MS, BSN, CCRA, CCRC

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Course Length Time 

2 hours; 12:00 - 2:00 p.m. Eastern

Course Dates 

December 15, 2010