- Gilead Sciences, Inc. (Foster City, CA)
- …of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave ... scientific and clinical leadership or input on activities including study protocol preparation, other study or investigator...scientific presentations. Scope may include phase 3 and 4 studies with an opportunity to contribute across studies… more
- Cedars-Sinai (Los Angeles, CA)
- …humankind?** The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol ... details, and participating in the informed consent process. Responsible for oversight of all studies with the group and the assignment of studies to clinical… more
- Stanford University (Stanford, CA)
- …candidates with outstanding communication and time management skills who are able to work independently on complex clinical research studies . Our staff run ... is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research… more
- Stanford University (Stanford, CA)
- …and patients with Alzheimer's disease, Parkinson's disease, and related disorders. These studies collect information on memory and other mental abilities, which we ... primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility of and… more
- Stanford University (Stanford, CA)
- …studies . **Duties include*:** + Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research ... inspect study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted… more
- Stanford University (Stanford, CA)
- …CRCA will perform duties related to the coordination of clinical studies , consent patients in person, interview patients, monitor follow-up, coordinate collection ... primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility of and… more
- Stanford University (Stanford, CA)
- …clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies . + Conduct study ... to implement study protocols with supervision. + Ability to provide work direction to research support staff. + Demonstrated understanding of good clinical… more
- GRAIL (Menlo Park, CA)
- …studies in support of GRAIL's robust clinical development pipeline. **Responsibilities:** + Work closely with GRAIL study team members to ensure that clinical ... we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to overcome one… more
- J&J Family of Companies (Irvine, CA)
- …of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for ; + Oversees/executes feasibility, selection, set up, conduct ... site management); + Contributes towards development of clinical trial documents (eg study protocol, informed consents, CRF, monitoring plan, study manual,… more
- Cedars-Sinai (Los Angeles, CA)
- …with the ability to read, write, and speak confidently. You will work closely with Spanish-speaking populations and must be comfortable engaging in conversations, ... conducting research activities, and providing study -related information in Spanish. Clear communication in both English and Spanish will be essential to support… more
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