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Janet Holwell, CCRC, CCRA, TIACR, FACRP
- Regulatory Affairs/Compliance
- Quality Assurance
- Clinical Research Administrators
Regulation states that ultimate responsibility for a clinical trial rests with the principal investigator. But what happens when a coordinator "goes rogue" and is guilty of misconduct? The speaker will explore the definition of misconduct in clinical trials and the possible consequences of intentional misconduct by a coordinator. Hear actual case studies delineating coordinator sanctions and punishments, as well as reasons for committing fraud.
4:45-5:00 Registration and Check in
6:00-6:15 Q & A
- Define Scientific Misconduct in Clinical Research
- List Three Cases of Coordinator Misconduct
- Describe the Consequences of Coordinator Misconduct
1 contact hour has been approved for through ACRP. Membership is not required for online registration/application of contact hours. Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
To receive contact hours: Purchase the contact hours, sign in at the registration desk and attend the program. Log on to the ACRP website then “My Courses” to complete the evaluation no later than 30 days following the event and obtain the online certificate. After 30 days, contact hours are no longer available.
Refund Policy: No refunds will be provided unless the chapter cancels program.