Join us for a workshop on research administration

October 26-27, 2017 - Charleston, SC

Learn how to accelerate your study start-up while maintaining billing compliance, obtaining the required funds for the study, and reducing risk exposure. 

Implementing and maintaining effective research administration practices can be difficult for any clinical trials office. Join PFS Clinical for a 1 ½-day workshop to gain valuable insights into all aspects of research administration. This workshop will include speaking sessions by our administration and compliance experts, case studies, and hands-on activities. Attendees can earn up to 11.1 CCB CEUs (Compliance Certification Board Continuing Education Units). Topics will include:

  • Billing Compliance
  • Coverage Analysis
  • Compliance Considerations for Budgets
  • High-Risk Contract Considerations
  • Efficient Study Start-Up and Negotiations
  • HIPAA for Research
  • Document Synchronization
  • Maintaining Compliance Throughout a Study


Register here.  For questions, contact or give us a call at (608) 664-9000 x 2264.

To pay by check instead of credit card, please fill out this form and email it to

Registration Rates:

  • Standard - $1,000.00/person
  • Non-Profit - $850.00/person

Who Should Attend?

This hands-on workshop is a must for professionals employed by academic health centers, hospitals, and university medical centers who work in research billing compliance, budgets/contracts, finance, and clinical trial management.

Attendees can earn up to 11.1 CCB CEUs (Compliance Certification Board Continuing Education Units)  by attending this workshop.



Marilyn Windschiegl, J.D.
Director, Clinical Research Contracts and Compliance


Amanda Miller, MS
Training Program Manager, Clinical Research Administration


Jody Ingebritsen-Howe
Manager, Clinical Research Contracts & Compliance


Liz Christianson
Senior Clinical Research Analyst