Clinical research billing (CRB) programs are required for all organizations participating in clinical research activities. This programs require the full understanding and application of applicable federal and state regulations governing clinical research activities. To be successful, organizations participating in clinical research activities should leverage technology to drive the daily operations and mitigate risk of non-compliance. The current complexity of the clinical trials requires innovation and optimization of technology platforms like the electronic health record (EHR).
WHY SHOULD YOU ATTEND?
Learn best and leading practices around optimizing and leveraging technology to build a compliant clinical research billing program.
AREA COVERED
- Optimal set up of electronic health records
- Optimizing technology to build compliance
- Best practice in clinical research billing
- Innovative ways of handling clinical trials requiring inpatient stays
- Downstream impacts of optimizing electronic health records for clinical research billing programs
- Streamlining budget development processes for clinical trials
- Working with clinical operations and revenue cycle personnel to achieve compliance with clinical research billing
LEARNING OBJECTIVES
- Optimizing technology platforms to deliver complex clinical trial treatments to patients.
- Leverage technology to enable delivery of complex clinical trial treatments to patients while maintaining compliance with insurance billing guidelines.
- Reduce the billing risk for sites and sponsors for clinical trials with inpatient stays.
- Speed up the delivery of novel compounds like CAR T cells to patients.
- Understand when to bill a sponsor vs. a patient's insurance for clinical trials with required inpatient stays.
- Streaming the budget development and negotiations for clinical trials with inpatient stays for patients.
WHO WILL BENEFIT?
- Compliance personnel at AMCs & Health Systems involved in clinical research
- Clinical study coordinators
- Clinical research nurses
- Clinical research finance personnel
- Patient billing personnel
- Pharmaceutical companies
Learn best and leading practices around optimizing and leveraging technology to build a compliant clinical research billing program.
- Optimal set up of electronic health records
- Optimizing technology to build compliance
- Best practice in clinical research billing
- Innovative ways of handling clinical trials requiring inpatient stays
- Downstream impacts of optimizing electronic health records for clinical research billing programs
- Streamlining budget development processes for clinical trials
- Working with clinical operations and revenue cycle personnel to achieve compliance with clinical research billing
- Optimizing technology platforms to deliver complex clinical trial treatments to patients.
- Leverage technology to enable delivery of complex clinical trial treatments to patients while maintaining compliance with insurance billing guidelines.
- Reduce the billing risk for sites and sponsors for clinical trials with inpatient stays.
- Speed up the delivery of novel compounds like CAR T cells to patients.
- Understand when to bill a sponsor vs. a patient's insurance for clinical trials with required inpatient stays.
- Streaming the budget development and negotiations for clinical trials with inpatient stays for patients.
- Compliance personnel at AMCs & Health Systems involved in clinical research
- Clinical study coordinators
- Clinical research nurses
- Clinical research finance personnel
- Patient billing personnel
- Pharmaceutical companies
Speaker Profile

Mary Veazie is a CPA and seasoned clinical research finance expert with more than 20 years of experience serving as the interface between principal investigators, clinical operations, and executive leaders in order to drive the development and implementation of clinical research program initiatives. Over the course of her career, she has been an innovative healthcare leader with a unique perspective in managing the financial aspects of the clinical research enterprise. She brings extensive experience in financial program management, financial modeling, and business plan development within the clinical trial space. Mary has a strong understanding of federal and FDA regulations governing the life …
Upcoming Webinars


50+ new Excel features so far this decade

Mindful Communication:The Key to Meaningful Conversations i…

FMLA Compliance in 2025: A Comprehensive Guide & Strategies…


Excel - 10 Key Worksheet Functions to Skyrocket Your Produc…

Managing Toxic Employees: Strategies For Leaders To Effecti…

Hiring and Retaining Employees in this Crazy Economy

Harassment, Bullying, Gossip, Confrontational and Disruptiv…

Project Management for administrative professionals


Excel Power Skills: Master Functions, Formulas, and Macros …

Outlook - Master your Mailbox - Inbox Hero Inbox Zero


Copilot and HR: An Introduction for HR Professionals


California Meal and Rest Breaks: What You Don't Know Can Co…

Bootcamp for New Managers and Supervisors: Develop These Es…

Policy Pops: Navigating DEI in the 2025 Workplace: Strategi…

Emotional Intelligence: Mastering the Emotions of Great Lea…


How To Conduct An Internal Harassment And Bullying Investig…

How to Manage the Legal Landmine of the FMLA, ADA and Worke…

The Importance of the first 5 seconds when presenting

Managing Difficult Employee Conversations

Female to Female Hostility @Workplace: All you Need to Know

How to Write Effective Audit Observations: The Principles f…


FDA Proposes Framework to Advance Credibility of AI Models