- BeOne Medicines (San Mateo, CA)
- …Disease Area Global Medical Affairs Plan. + Develop and execute on a data generation strategy outside of the clinical development program, including investigator ... on disease area advisory meetings. + Interpret, and present clinical trial data both internally and externally....of, author, update, and/or review. + Train BeOne colleagues, CRO staff, and study site staff on the therapeutic… more
- BeOne Medicines (Emeryville, CA)
- …from sites, IRBs/IECs, Health Authorities, and CRO 's + Review, query, and analyze clinical trial data + Interpret, and present clinical trial data ... The Vice President will support BeOne Medicine's Clinical and Medical assets within the Hematology franchise...franchise by successful development of early and late phase clinical development strategies and deliverables in partnership across the… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …trend review for safety signals from ongoing trials + Interpret, summarize, and present data from clinical trials to the company and externally + Provide ... and regions. **Position Overview:** The Medical Director will be responsible for clinical strategy relating to upcoming clinical trials, including indication… more
- BeOne Medicines (Emeryville, CA)
- …global clinical studies + 8 or more years of progressive experience in clinical research within biotech, pharma or CRO industry + Proven project management ... within agreed timelines and budget + Leads all aspects of assigned clinical study(ies) + Leads global cross-functional study team (including oversight of external… more
- BeOne Medicines (Emeryville, CA)
- …Applications **Other Qualifications:** + 6 or more years of progressive experience in clinical research within biotech, pharma or CRO industry + Proven ... across a program as required + Leads the regional clinical operations team (including external partners working on a...study for countries in region + Manages the trial data collection process for the region, drives data… more
- Edwards Lifesciences (Irvine, CA)
- …your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how ... our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase… more
- BeOne Medicines (Emeryville, CA)
- …Excel, PowerPoint, Teams and Outlook + Familiar with industry CTMS and data management systems **Other Qualifications:** + Understands clinical trial processes ... quality of trip report, action item management, query management, data currency and TMF management + Responsible for managing...and TMF management + Responsible for managing relationship with CRO FSP line manager and liaising to understand and… more
- Norstella (Sacramento, CA)
- …**About Citeline:** Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices ... Clinical Solutions combining platform, services and Real World Data (RWD) offerings to support use cases across the...activities **Qualifications:** * 5+ years experience in working in clinical trial relevant business either CRO , trial… more
- Charles River Laboratories (Northridge, CA)
- …Certification (eg, ASQ certification in auditing, SOCRA, CRS or Association for Clinical Research Professional) highly preferred. Compensation Data The pay range ... * Perform internal and external supplier audits. * Manage the inspection/back room during regulatory or customer audits. * Review validation reports (IQ/OQ/PQ) *… more
- San Jose State University (San Jose, CA)
- …the following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs, clinical and medical affairs, quality ... experience in a medical device, pharmaceutical, In Vitro Diagnostics, and/or Clinical Research Organization ( CRO ) or a Ph.D. in a relevant discipline with 0-2… more
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