Study & Site Management Journey

Learn practical, proven ways to maximize study and site performance.

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

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