- Amgen (Thousand Oaks, CA)
- …product lifecycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory , and medical affairs They will ... tissue expansion, and proptosis, improving both functional and quality-of-life outcomes. Clinical studies have demonstrated its efficacy and safety across patients… more
- Cedars-Sinai (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... enduring, precision treatment to patients around the world. The Clinical Research Associate I works directly with a ...for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including… more
- University of Southern California (San Diego, CA)
- …in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s). Duties ... Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical -Research-Associate\_REQ20160224/apply) Keck School… more
- J&J Family of Companies (Santa Clara, CA)
- …cross functional teams including but not limited to R&D, Supply Chain/Manufacturing, Clinical and Medical Affairs, Regulatory Affairs, Service, Marketing, in ... and industry standards including customer safety and satisfaction and regulatory compliance with business objectives. + Prioritize and resource benchmarking… more
- Pfizer (South San Francisco, CA)
- …and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + ... working in a matrix team environment with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists. Meet… more
- Cedars-Sinai (Los Angeles, CA)
- …and research objectives. Position is responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... with an organization known nationally for excellence in research!** **Job Summary:** The Clinical Research Associate I works directly with a Clinical Research… more
- Cedars-Sinai (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... **Job Description** The Clinical Research Associate I works directly with a...for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including… more
- Cedars-Sinai (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... plus, it is not required-transportation will be provided for outreach travel. The Clinical Research Associate I works directly with a Clinical Research… more
- Cedars-Sinai (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... an organization known nationally for excellence in research!** **Job Responsibilities** The Clinical Research Associate II works directly with a Clinical … more
- Cedars-Sinai (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the ... **Job Description** **Key Job Responsibilities** The Clinical Research Associate I works directly with a...contact for long term follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board (IRB) including… more