8:00-8:30am
Tuesday, July 30, 2019 – Staff
Registration & Breakfast
8:30-9:20am
Keynote: Working Toward a Cure in Hemophilia
Description to come
Speaker
Barbara Konkle, MD
Barbara Konkle, MD9:30-10:30am
The Human Research Protection Program: Cultivating a Partnership with your IRB
Institutional Review Boards (IRBs) have a federal mandate to facilitate research that protects the rights, safety, and well-being of research participants. By establishing a collaborative relationship with your IRB office, you can minimize misunderstandings, efficiently move your studies through the work flow, and together promote safe, ethical, high quality research.
Speaker
Adrienne Meyer, MPA, CIP
10:40-11:40am
The Clinical Research Billing Cycle: Staff Role in Research Budget
The clinical research billing cycle is a complex process that involves multiple offices billing both clinical and study tests to the patient and the study budget. This session will provide an overview of a typical clinical research billing cycle, and highlight hand-offs between billing offices and members of the research team to prevent errors.
Speakers
Will Dean
Eli Reis
Laurel Weigler
11:40am-1:00pm
Lunch Break
1:00-2:00pm
Clinical Trial Management Systems: A One Stop Solution
Clinical Trials Management Systems (CTMS) integrate the multiple components of clinical research, such as billing, implementation timelines, and reporting guidelines. This session will describe the role of a CTMS and give a demonstration of the CTMS that will be rolled out at UW, SCCA, and Fred Hutch.
Speaker
Oscar Cano
2:00-2:15pm
Break
2:15-3:15pm
Accelerating Study Initiation: Institutional Resources to Catalyze Study Design
Learn sound methods to determine how best to approach implementing a new study, and apply elements of project management to organize the financial, timeline, institutional oversight, and research support resources to move your study through the start-up process.
Speaker
Ashley Waldie, MA, CCRP
3:25-4:25pm
An Ethical Framework for Clinical Research: Rethinking and Going Beyond Informed Consent
In this session you will learn about eight ethical benchmarks for clinical research and apply them to cases to understand the trade-offs involved in ethical analysis.
Speaker
Ben Wilfond, MD
