- System One (Walnut Creek, CA)
- …(approximately 5-10 hours per week) Onsite Requirement: Yes Overview The Clinical Research Sub - Investigator (SI) supports the Principal Investigator in the ... Gastroenterology, and Rheumatology focus) required/preferred. + Prior experience as a Sub - Investigator or Clinical Research Physician strongly desired. + Good… more
- System One (Walnut Creek, CA)
- …Rheumatology focus) required/preferred. + Minimum 5 years of experience as a Principal Investigator or Sub - Investigator in clinical research. + Strong ... Job Title: Clinical Principal Investigator Location: US Based - Remote Engagement Type...informed consent forms, and case report documentation. + Supervise sub -investigators, research coordinators, and clinical staff to ensure GCP… more
- Cedars-Sinai (Beverly Hills, CA)
- …of regulatory/IRB operations from start-up to closeout. + Serves as sub /co- investigator on clinical trials, observational research, and biobanking protocols. ... activity, research manuscript publications, program progress narratives, scientific highlights, investigator 's, other support, young investigator awards, Core… more
- Bristol Myers Squibb (San Diego, CA)
- …to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and ... regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...time. **Education and Experience** + MD or equivalent with sub -specialty training in oncology and at least 8 years… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Project Teams and represent Global Therapeutic Area Regulatory on cross-functional core and sub -teams. You will typically serve as a Gilead contact to / for ... Affairs and cross-functional leaders and teams. + May participate on other Sub -teams (eg, Study Management, Clinical, Nonclinical, Biomarkers) or assign such to… more
- Bristol Myers Squibb (San Diego, CA)
- …of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial ... and regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits with clinical trial investigators + Execute and deploy… more
- J&J Family of Companies (Irvine, CA)
- …Learn more at https://www.jnj.com **Job Function:** R&D Operations **Job Sub ** **Function:** Clinical Trial Project Management **Job Category:** Professional **All ... study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …generation of medical evidence, (eg, observational studies, registries, and investigator -initiated studies (IISs) / investigator -initiated trials (IITs)) + Manage ... dashboards + Coordinate and communicate with key Global Medical Affairs sub -functions such as PASM (Patient Advocacy and Stakeholder Management) and Medical… more
- J&J Family of Companies (Irvine, CA)
- …Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub ** **Function:** Medical Affairs **Job Category:** People Leader **All Job Posting ... evidence generation and dissemination strategies for company sponsored and investigator initiated research. + Collaborate with evidence generation colleagues from… more
- J&J Family of Companies (Irvine, CA)
- …at https://www.jnj.com **Job Function:** Discovery & Pre-Clinical/Clinical Development **Job Sub ** **Function:** Clinical Development & Research - Non-MD **Job ... (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports); . Ensures applicable trial registration (eg on… more