North Texas Chapter: 2024 Fall Symposium
Event Description:
This program is designed to discuss preparedness in the conduct of clinical research by highlighting key laws & regulations that affect the research industry; how trial site managers can be fair & equitable with their teams in terms of workload expectations & barriers to communication between providers, patients, and families.
Speakers:
Richard Dima, MD, MBA, CCRC
Senior Director, Clinical Research
Office of Clinical Research
Northwell Health/Lake Success, NY
David Vulcano, LCSW, MBA, CIP, RAC, FACRP
Vice President, Clinical Research Compliance & Integrity
HCA Healthcare/Nashville, TN
Learning Objectives:
- Learn to develop a workload assessment tool for your research staffing needs, how to calculate acuity results & how it can improve employee satisfaction & retention
- Understand relevant portions of the various laws, regulations and guidance, & potential impact to the research industry
Registration Information:
This event is $40 to attend. Click here to register.
Contact Hour Information:
This event will over 4 contact hours. Click here to purchase your contact hours. Please purchase and claim your contact hours by 11/5/2024.
- Chapter Member: $0
- ACRP Member: $25
- Non-Member: $40
To receive contact hours: Purchase the contact hours and attend the program. After attending the event, log on to the ACRP website and visit learning.acrpnet.org, click “GO TO MY COURSE”. Select your event, confirm attendance and take the event evaluation between 1 and 30 days following the event and obtain the online certificate. After 30 days, contact hours are no longer available.