November 2024 SOCRA Source Journal - Journal - Page 2
TABLE OF
CONTENTS
PRESIDENT’S MESSAGE ....................................................... 4
SOCRA INFORMATION
BOARD OF DIRECTORS .........................................................5
SELF-STUDY OPPORTUNITY
2024 ANNUAL CONFERENCE
Informed Consent: Guidance for IRBs,
Clinical Investigators, and Sponsors ....................................... 6
Self Study Questions ............................................................. 10
Self Study Answers ................................................................ 21
JOURNAL ARTICLES
Enhancing Patient Recruitment in Clinical Trials through
Arti昀椀cial intelligence: A Comprehensive Review
Ijeoma Oyegunle MD., MPH ..................................................... 11
Developing a Research Financial and Billing
Compliance Plan
Tracy Popp, MBA, CHRC, CRCP, CCRP ..................................... 23
Notes to File: Compliant Practices to
Ensure Data Integrity
Heather Pham, MS, CCRP, CHRC .............................................. 27
Proper Documentation of a Clinical Trial: What Are
All These Forms and How Do I Complete Them?
Laura Adkins, MAP, CCRP, CCRA, CRS, AdvCRS ....................... 37
Perspectives of a Post-Baccularate Program Advancing
Diversity, Equity, and Inclusion in Pediatric Clinical Research
and Professional Pathways
Joanna Ly, BA ............................................................................ 61
Clinical Site Monitoring in the Time of COVID-19 and
Beyond: Best Practices in Remote Site Monitoring on
the ACT NOW Trials
Lauren N. Bradley, MHS; Margaret Crawford, BS;
Lillian Trochinski, RN, BSN ......................................................... 67
2
SOCRA SOURCE © November 2024
33rd Annual Conference in Review..........76-79
Poster Winners ............................................ 76
Poster Winner Abstracts ..........................80-81
CHAPTER PROGRAM
Chapter Contacts ................................... 82-83
CERTIFICATION ............................... 84-86
Eligibility ...................................................... 86
Maintaining Certi昀椀cation ............................. 86
CONFERENCES AND WORKSHOPS
Online Educational Programs.......................87
FDA Clinical Trials Requirements ................. 88
Site Coordinator / Manager Workshop ....... 89
Certi昀椀cation Prep & GCP Review Course .... 90
Clinical Research Nursing Conference ........ 91
Emergency Clinical Research Symposium ... 92
Advanced Site Management:
Finance & Productivity Workshop................ 93
Pediatric Clinical Trials Conference ............. 94
Clinical Research Monitoring Conference ... 95
Program Management Virtual Conference .. 96
Oncology Clinical Trials Conference............ 97
Decentralized Clinical Trials Conference ..... 98
Device Conference ...................................... 99
‘Hot Topics’ for Protecting Human
Research Participants Workshop ............... 100
Program Management Conference ........... 101
Educational Opportunities ........................ 102
ADVERTISING OPPORTUNITIES
Print and Web Advertising ........................ 103
