Safety Event Identification by Clinical Research Nurses
Speakers: Jennifer M. Gabany, CRNP, MSN, CCRC; Nat’l Research Nurse Coord., VABHS
Annette M. Phillips, BSN, CCRC; Research Nurse Coordinator, VABHS
Registration Cost: Free for all to attend.
Program Agenda:
- 5:00 – 5:15 pm – Arrival & Registration
- 5:15 – 5:30 pm – Chapter Updates
- 5:30 – 6:30 pm – Presentation and Q&A
Program Description: This program provides an overview of safety reporting for clinical trial compliance focusing on the local reporting process. In the context of an multicenter, randomized trial, the speakers discuss disparities in compliance and discrepancies of unreported events identified in routine auditing and remote EMR review. research study is described for exploring the process utilized by clinical research nurses to identify events that may impact the safety and welfare of research participants.
Upon completion of this presentation, attendees should be able to:
- Describe the safety reporting requirements for local research compliance;
- Explain the design of a qualitative research study using grounded theory methods;
- Be able to discuss the impact of research coordinators on safety event reporting.
Target Audience: Open to all Clinical Research Professionals, students interested in Clinical Research
Contact hours: 1.0 contact hour has been approved through ACRP.
To receive contact hours: Purchase the contact hours, sign in at registration or in the webcast, and attend the program. Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
Further Information: Contact Romiya Barry at nec.acrp@gmail.com or call 508-264-0113.
Refund Policy: Contact ACRP member support
Level: Intermediate