Waiting List For: Recruiting, Consenting and Enrolling Study Subjects (2/14/13)
Thursday, February 14, 2013 8:30 AM - 12:30 PM
This workshop is for the research coordinator with 2+ years of experience and provides detailed information on the expectations and processes for recruiting, consenting, and enrolling subjects into clinical trials.
Proper enrollment of study subjects leads to GCP compliance and meaningful clinical data. Research nurses and CRCs who fully comprehend the correct methods for recruiting and enrolling subjects as well as the consequences of improper enrollment can significantly and positively impact the trials they run.
Appropriate techniques and recommended sources for identifying potential research subjects will be explained. The regulations and guidance documents applicable for consenting and enrolling subjects will be reviewed. Best practices for tracking all aspects of this process will be explored, with examples from industry-sponsored and investigator-initiated studies. Participants will bring their own experiences to engage current practice and assumptions against regulatory requirements. A hands-on exercise will reinforce the skills taught at this workshop.
Fee: $125 (includes refreshments, material, certificate of completion)
Cancellation Policy: If you are no longer able to attend, please cancel your registration by Thursday, Jan. 31, 2013 for a full refund. Contact firstname.lastname@example.org thereafter.