Clinical Trials
Information for Investigators new to Virginia Mason Medical Center
- Ethics/GCP Training (all key personnel) must be completed prior to approval.
- Submit BRI / Investigator Compact. Send to Cheryl Weaver, IN-RC.
Key Personnel: Persons responsible for one or more of the following:
- Day-to-day protocol decision-making related to the study conduct;
- Participant recruitment, selection and eligibility;
- Clarification of the complexities of the protocol to the participant and others;
- Collecting participant information and entering data using procedures to maintain privacy and confidentiality;
- Ensuring that the rights and welfare of participants are monitored throughout the study.