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Study Staff
Resources for Study Staff
Last revised
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06/11/2024
Pre-Study
Informed Consent Development
Coordinator Training
Good Clinical Practice
iRIS / IRB Submissions
Recruitment Strategy
Coverage Analysis
Clinical Trial Budgeting
Study Set-Up
Cancer Research Activation Workflow (USA and international studies)
Regulatory
21 CFR Part 11 Compliance
Clinical Trials.Gov
Data & Safety Monitoring
IND Development
IDE Development
Regulatory Binder
SOPs
Study Management
Data Management
Research Billing
Specimen Management
Clinical Labs Research Specimen Transportation Service
Study Management
Subject Enrollment
Quality Management
UCSF Care Everywhere and Research Policy for Clinical Research Coordinators