- Kelly Services (San Ramon, CA)
- …contact lenses. + Aware of basic regulatory requirements related to medical devices (GCP/ IRB / Design Control/ FDA & ISO standards/ EU MDR, etc.) and applies ... knowledge under direction of clinical management. + Conducts basic clinical assessments; serves as Sub-Investigator under direction of Principal Investigator. + Actively apply learnings from prior experience, current trends in clinical research, and competitor… more
- UCLA Health (Los Angeles, CA)
- …content, communications, and other materials. This may include works related to IRB protocol submission and approval. + Supporting the effort to ensure compliance ... with all UCLA as well as relevant federal and state regulations. + Collaborating in works toward the completion of all program/project activities, research, outreach, and recruitment. Work with research participants on consent and surveys/interviews. +… more
- 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 legal requirements while maintaining competitive positioning, and advise on permissible health… more
- Stanford Health Care (Redwood City, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. **Locations** Stanford Health Care **What… 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 ... Stanford Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. This job description covers all… 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 ... Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. **Locations** Stanford Health Care **What… more
- Stanford University (Stanford, CA)
- …and in close collaboration with MCHRI and the program's Scientific Advisory Board , the Program Manager will be responsible for advancing the vision, strategy, ... program, including the development of funding opportunities, oversight of application and review processes, and coordination of progress reporting. In this role, the… more
- Oura (San Diego, CA)
- …do: + Lead cross-functional research study execution-including budgets, contracts, IRB and regulatory submissions, logistics, trouble-shooting, and data quality ... our network of research partners-identify, vet, and build relationships with institutional partners and CROs to complement our internal capabilities + Collaborate… more
- Cedars-Sinai (Los Angeles, CA)
- …meetings and recruitment meetings. Intern will be working with CS-link for chart review , research database, and specimen samples. The intern will officially be added ... to the IRB study and have taken CITI Training, making this allowable. Intern will assist clinical trial staff to gather non-invasive study assessments and enter… 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 ... work the following day. I. Outpatient / Clinic: 1. Review clinic charts, pre clinic, and order any additional...and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee. This job description… more