Name
Special Issues in Oncology Clinical Trials Breakout: Best Practices for Sites Interested in Conducting Phase 1 Oncology Studies
Date & Time
Tuesday, October 18, 2022, 10:45 AM - 11:30 AM
Location Name
Melrose 4
Description
This session will focus on best practices for sites that are interested in starting a phase I research program. There will be a site and sponsor perspective for this session.
Speakers
Cheryl Sampson - Director, Clinical Research Office - University of New Mexico Comprehensive Cancer Center
Ann Lovelace - Director, Research Operations - Comprehensive Cancer Centers of Nevada
AnaArlene Ramirez - Manager, Phase I Research Operation - Comprehensive Cancer Centers of Nevada
Renee Smith - Head, ED Oncology Capabilities and Alliances - Janssen
Ann Lovelace - Director, Research Operations - Comprehensive Cancer Centers of Nevada
AnaArlene Ramirez - Manager, Phase I Research Operation - Comprehensive Cancer Centers of Nevada
Renee Smith - Head, ED Oncology Capabilities and Alliances - Janssen




Learning Objectives
- Describe sponsor expectations for Phase 1 study sites
- Identify site staffing needs, site facility requirements, site contracting/budgeting/vendor requirements, site clinical requirements, and Phase 1-specific requirements/considerations.
This Module is Eligible for
ACRP CE Points, CCB Credits, CLE Credits, CME Credits, CNE Credits
ACRP CE Points
0.75