- Gilead Sciences, Inc. (Foster City, CA)
- …thinking in advising others on statistical requirements and opportunities to improve study or other project outcomes. + Understands drug development phases ... document review and data inclusion for NDA submissions of assigned studies by collaborating with cross-functional partners to meet clinical development project… more
- Cedars-Sinai (Los Angeles, CA)
- …patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all ... team!** The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol eligibility,… more
- Stanford University (Stanford, CA)
- …in Radiation Oncology. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies . ... and flexibility. **Duties include*:** + Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research… more
- Bristol Myers Squibb (San Diego, CA)
- …organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, ... external network + Manages Phase 1 - Phase 4 studies , with demonstrated decision making capabilities + Provides medical...and is a key member of a high performing Study Delivery Team (SDT) and may be a member… more
- Merck (South San Francisco, CA)
- …I studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug ... for planning and management of an important inflection point in the drug development process, working closely with scientific, regulatory, statistical, and modelling… more
- Gilead Sciences, Inc. (Foster City, CA)
- …monitor and engage with external investigators to ensure timely execution of contracted studies + Create study metric trackers + Review abstracts and/or ... hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure...manuscripts that result from supported studies + Support closure of studies when… more
- BeOne Medicines (San Mateo, CA)
- …up to 2 studies in late development) + Seamless transition of drug candidates from research to early clinical development + Effective integration of in-licensed ... + Provides leadership and clinical oversight across all assigned studies and programs (up to 2 programs in early...drug candidates into early clinical development portfolio + Effective… more
- Cedars-Sinai (Beverly Hills, CA)
- …patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all ... Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility,… more
- Cedars-Sinai (Los Angeles, CA)
- …patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all ... Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility,… more
- Cedars-Sinai (Los Angeles, CA)
- …Program Administrator, or Research Nurse to coordinate and/or implement the study . Evaluates and abstracts research data and ensures compliance with protocol ... the IRB. Provides limited patient contact as needed for study and assist with study budget and...all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. +… more