- 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 ... manuscripts that result from supported studies + Support closure of studies when...of global investigator-sponsored research (ISR) and collaborative Phase IV study proposals + Act as a resource of Phase… more
- Gilead Sciences, Inc. (Foster City, CA)
- …clinical supply for the overall development portfolio, including clinical development programs and studies at all phases as well as managed access programs. May lead ... and robust resource allocation for PDM sub-teams and clinical study teams. + Partners across several PDM functions and...(OTIF) delivery of IMP to initiate and resupply clinical studies . + Responsible for decision-making and direct the long-term… more
- Parexel (Glendale, CA)
- …the Early Phase Clinical Unit (EPCU). + Assume responsibility for patient care and study conduct assignments. + Ensure that all study laboratory and medical ... completed, and that eligibility requirements specific to the assigned study are met. Assess compliance, symptoms, etc. per ...Act as participant advocate in the conduct of clinical studies . **Qualifications** + At least 2 years working in… more
- AbbVie (Irvine, CA)
- …markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff. *May have ... responsibility for leading clinical study teams, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining… more
- Bristol Myers Squibb (San Diego, CA)
- …the internal and external network + Manages Phase 1 - Phase 4 studies , with demonstrated decision making capabilities + Provides medical and scientific expertise to ... and is a key member of a high performing Study Delivery Team (SDT) and may be a member...Provides oversight and medical accountability for a group of studies + Leads the analysis of benefit/risk for clinical… more
- Merck (Sacramento, CA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial… more
- Taiho Oncology (Pleasanton, CA)
- …of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting of clinical trials. Performance Objectives: + Collaborates ... the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs),...and leverages the knowledge for designing and summarizing clinical studies . + Keeps Sr. Medical Director current on status… more
- Bristol Myers Squibb (San Diego, CA)
- …responsible for the design, implementation, monitoring, analysis, and reporting of studies conducted within RayzeBio's portfolio to ensure the program meets the ... and partner with investigators and CROs to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study… more
- City of Long Beach (Long Beach, CA)
- …of the annual budget; performs preliminary research, investigations, and studies ; develops preliminary interpretations and makes recommendations for improvement in ... on the form. Degrees must indicate the field of study and transcripts must indicate the field of ...Insurance . Life Insurance . Retirement Plan (PERS) . Paid Vacation, Personal Holidays and Sick Leave . Deferred… more
- AbbVie (Irvine, CA)
- …and creatively apply methodology and analytical skills to bring resolute answers through novel study design. The position may be filled at either the Director I or ... in Irvine, CA. Key Responsibilities + Define objective and develop study design scenarios/options to support novel non-interventional and interventional studies… more