Budgeting and Billing Compliance in Study Activation
Wrongfully billing items and services to a participant’s insurance is an ever-growing risk in clinical research. Additionally, obtaining the necessary funds for an industry-sponsored clinical trial can be daunting. This can be particularly challenging for smaller research sites, who may not have dedicated internal teams to manage such financial risk. Finding personnel who know insurance statutes and clinical trial financing can be a challenging and costly undertaking.
Join Advarra’s Business Operations Services Manager Jake Meyer as he discusses common strategies sites take to protect themselves from such financial risks. From making do with a tight budget to taking less conventional approaches, learn how you can ensure that reliable timelines are maintained, even amid fluctuations in demand.
- Outline how research sites can protect themselves from billing-related audits and lawsuits
- Identify best practices sites can obtain necessary funds from a clinical trial
- Discuss trends leading to success in budgeting and billing compliance
Business Operations Services Manager
Who should watch?
This content applies to representatives from research institutions, including coverage analysis experts, budget and contract team members, clinical trial operations team members, and research administration staff, as well as representatives from sponsor/CRO organizations, including clinical research managers and budget and contract team members.
Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.
Provider approved by the California Board of Registered Nursing, Provider Number 17600, for 1 contact hour. This documentation must be retained by the licensee for a period of 4 years after the course concludes.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.
If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.
Certificate of Attendance
After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.
DATE: October 21, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour