Are you involved in the registration, management, and results entry of studies in the Protocol Registration and Results System (PRS)? Are you struggling with how to start and where to go for help? The workshop will review PRS Administrator responsibilities, lessons learned from moving an existing program toward a positive direction, and provide guidance for managing trials, in addition to reviewing the registration and results entry process. Best practices and helpful tips for both Administrators and users will be provided. Attendees are invited to bring their own scenarios for group discussion and should leave the workshop with skills to successfully manage trials within ClinicalTrials.gov.
- Stacey Arnold, PhD (Results Team Subject Matter Expert, ICF/NIH)
- Cristina Ferrazzano Yaussy, MPH, CCRP (Research Regulatory Analyst, Darmouth-Hitchcock Medical Center)