St. Louis Chapter: The Sponsor’s Role in Relieving the Burden of Remote Monitoring on Sites (ACRP 2024 Conference Replay)
This event will be presenting a session replay from the ACRP Conference Library
Event Description:
While eRegulatory (eInvestigator Site File) systems favored by study sponsors offer many advantages to sites, their adoption and use may place burdens on site personnel that can be alleviated with careful planning and collaboration between partners. Speakers in this session will share specific use cases where the use of eRegulatory has made a positive impact on clinical trials, as well as overall metrics on site adoption, user feedback from site and sponsor roles, and lessons learned and future opportunities for both study coordinators and monitors.
Speakers:
- Dan Knight, Associate Director of Clinical Research, Merck
- Kayla Perry, Clinical Research Associate, Merck
Event Agenda:
Welcome and chapter business: 10 minutes
Content replay: 1 hour
Discussion: 20 minutes
Registration & ACRP Contact Hour Information:
- Chapter Member (registration with or without contact hours): $0
- ACRP Member (registration only): $0
- ACRP Member (registration + contact hours): $15
- Non-Member (registration only): $15
- Non-Member (registration + contact hours): $45
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To claim contact hours: Register and purchase the contact hours and attend the event. After attending the event, visit learning.acrpnet.org and log into your ACRP account. Click the “GO TO MY COURSES” box. Find the event in your dashboard, confirm your attendance, and take the event evaluation between 1 and 30 days following the event to obtain the online certificate. After 30 days, contact hours are no longer available.