- University of Southern California (Los Angeles, CA)
- …reporting of Serious Adverse Events. Enters SAE into iStar for reporting to the IRB . Notifies Data Managers promptly of occurrence of SAE. 5. Interacts with the ... monitors/auditors from the sponsoring pharmaceutical companies. B. Protocol Administration 1. Determines patient eligibility a. Schedules necessary tests. b. Ensures that written informed consent is obtained using correct version of the stamped Informed… more
- Stanford University (Stanford, CA)
- …to work as it maintains the highest level of scientific rigor, institutional support and coordination for the complete range of cancer-related research, including ... multidisciplinary teams across different faculties or schools. + Perform ongoing literature review to remain current with new procedures and related research; apply… more
- Stanford University (Stanford, CA)
- …our team. Based on the applicant's education and experience, Human Resources will review and verify qualifications to determine the appropriate level. As a (Senior) ... level based on the applicant's education and experience. Human Resources will review and verify the stated qualifications of the selected applicant to determine… more
- Stanford University (Stanford, CA)
- …. Will be expected to assist with regulatory aspects of animal research, including IRB submissions or APLAC protocols. . Plan approach to experiments in support of ... procedures and protocols in collaboration with senior researcher and lab members. . Review literature on an ongoing basis to remain current with new procedures and… more
- Stanford University (Stanford, CA)
- …available datasets and registries, from the National Institutes of Health, multi- institutional collaboratives, and various other sources. . Obtain and harmonize ... with all local and external regulatory and privacy requirements, including the IRB , funding agencies, and database guidelines. . Devise and implement data quality… more
- Stanford Health Care (Palo Alto, CA)
- …initiation visits. + Supports practices relating to pharmacy dispensing based on IRB approved clinical trials. + Provides guidance to investigational drug service ... major contraindications and potential side effects. **Licenses and Certifications** + CA Board of Pharmacy License - Registered Pharmacist required . and + BLS… more
- University of Southern California (Los Angeles, CA)
- …of regulatory and protocol materials to support clinical research studies (eg, IRB applications, study protocols, SOPs) would be a particular asset. Strong ... quantitative skills would also be a highly valued asset for this position. The annual base salary for this position is $70,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the… 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
- Providence (Fullerton, CA)
- …responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB . This position is directly responsible to ensure that all documentation is ... timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simply valued - they're invaluable. Join our team at Providence Medical Foundation and thrive in our culture of… 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