Facilitate Clinical Trials and Translational Research by Providing Centralized Regulatory, Financial, and Administrative Support to all Cancer Center Investigators
Protocol Development: Consultation and Development
Regulatory Document Preparation and Maintenance
Study Initiation, Auditing and Monitoring Assistance
Centralized Safety and Protocol Violation Reporting
Provide Research Support Services for Cooperative Group Studies
Cooperative Group Regulatory Assistance and Audit Preparation
Cooperative Group Study Coordination and Data Management Assistance
Centralize and Standardize Data Collection and Reporting of Clinical Research
OnCore Database
Report Generation
Electronic Case Report Forms for Investigator Initiated Trials
Provide Programs to Contribute to Quality Assurance of Performance and the Ongoing Education of Cancer Center Clinical Research Personnel
Clinical Research Staff Hiring, Orientation and Training
Quality Assurance Program
Standard Operating Procedures Development and Maintenance
Monthly Educational Programs for Research Staff
Mandatory Training Prior to Commencing Each Investigator-Sponsored Trial
Annual Clinical Research Forum for Research Staff and Community Affiliates
Clinical Trials Forums
Newsletter
Coordinate Outreach Efforts in the Community to Increase Clinical Trials Awareness
and Accrual
Protocol Listings
Clinical Trials Phone Line
Programs to Increase Awareness and Accrual to Clinical Trials
Outreach Program
Administration of an ECOG Affiliates Program
Multidisciplinary Management of Cancers: A Case-Based Approach CME Meeting
Promote Interdisciplinary Collaborations and Translational Medical Research
Trial Administration