- Oura (San Francisco, CA)
- …legal and regulatory oversight for clinical studies and evidence generation, including IRB approvals, informed consent, and compliance with FDA, Common Rule, EU MDR, ... and GDPR requirements for human subjects research , and retrospective studies. + Oversee labeling and marketing compliance, ensuring that product claims align with… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... clinical care for the sickest, most vulnerable patients and performing cutting edge research to bring discovery to the bedside and improve patient outcomes. The APP… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... settings + Participate in service development, quality improvement initiatives, and research data collection + Provide cross-coverage support and flexibility to… more