Leveraging Data to Lead and Manage the Research Mission: Data-Driven Decision Making at all Levels of the Organization
This webinar discusses how an organization uses data at all levels to lead and drive the research enterprise and day-to-day operations.
Durham Nephrology Associates Enhances Reporting and Patient Experience Using CCPay
Learn how Durham Nephrology Associates implemented Advarra CCPay to enhance their clinical trial staff and patient payment process experience.
Beginner’s Guide to Independent Asset Reviews
Learn more about independent asset reviews and how they can enhance research operations.
Maintaining a Robust Clinical Trial Pipeline
Explore how the COVID-19 pandemic has changed the clinical trial landscape and how it affects the business pipeline.
Why it is Critical to Have and Enforce a Data Strategy?
Understand a data strategy's role in clinical research and how enforcing one will benefit your studies.
Do You Have Appropriate Oversight? Understanding the Role of DSMBs
Take a look at the role and function of independent DMCs from charter creation through interim data analysis to prepare your next trial.
Optimizing a Clinical Development Program to Improve ROI
As a clinical trial moves through phases, how does the return on investment benefit study design and the program overall?
Site-Driven Metrics: Operational Data To Improve Research
Most metrics are geared toward sponsors and CROs, find out how this ultimately impacts site research operations
DMC vs IRB: What’s the Difference?
In a complex clinical trial, data monitoring committee's oversee interim data to ensure adequate safety monitoring.
Improving Study Activation Time for Gene Therapy Research
With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts
The Current State of Study Activation and Methods to Ensure Success
This webinar will discuss the importance of protocol feasibility and identifying solutions to ensure your organization's success.
The State of Clinical Trial Activation at Sites
While the study activation process is necessary for all sites to conduct, efficiently coordinating all necessary aspects can be challenging.