Study & Site Management Track

Clinical study site teams will gain practical strategies and expert guidance to elevate clinical trial execution, streamline monitoring, and deliver high-quality outcomes.

 
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Perfecting the Science and Art of Staffing for Clinical Trials
Defining the Role of the Clinical Research Associate in Site-Sponsor Relationships
The Hidden Costs of Diversity and Inclusion in Clinical Research
Transforming Stipend and Reimbursement Practices for Trial Participants
Assessing and Managing Study Coordinator Workload
Back to Clinical Trial Budgeting Basics: Are Your Costs Covered?
Detecting and Addressing the Quality Pitfalls at Study Sites
Managing the Consequences of Audits and FDA Inspections
The ABCs of Risk-Based Monitoring for Sites
Investigator Compensation: One Size Does Not Fit All
Clinical Trial Diversity & Intersectionality: Looking at the Whole Patient
Best Advertising Practices and Partnerships for Patient Recruitment Success
Data-Driven Protocol Feasibility to Improve Research Productivity
A Site Management Organization Approach to Study Start-Up
Starting from Scratch to Establish an Investigator-Initiated Research Program
Novel Clinical Research Recruitment Models Developed in Partnership with Sites
Innovation in Investigational Product Management
Assessing and Sustaining Your Community Engagement Plans and Partnerships
Keeping Up with the FDA's Changing Ways
Project Management Skills for Accelerating Study Start-Up
Cautionary Tales from the Front Lines of Clinical Trials
Ensuring Trial Accessibility for Deaf Participants
Building Clinical Trial Research Capacity at Community Cancer Centers
ACRP Game Show: Fun Facts with Friends
Addressing Health Inequities in Clinical Research
Challenges and Solutions for Getting Physicians Involved in Clinical Trials
Should Your Patient Recruitment Engine be Gas, Electric, or Hybrid?

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