- Cedars-Sinai (Los Angeles, CA)
- …guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies . + May assist with grant proposals, ... Nurse Coordinator III is responsible for all activities associated with clinical study coordination, subject enrollment, data management/integrity, regulatory… more
- AbbVie (South San Francisco, CA)
- …Mondays and Fridays. Responsibilities + Aligns DSS study teams with program- and study -level strategies. For assigned studies , leads the DSS Study Team ... process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through...and represents DS as a member of the cross-functional study team + For assigned studies , acts… more
- AbbVie (South San Francisco, CA)
- …program- and study -level strategies. Supports governance of assigned programs and studies , both within and outside DSS. Assigned programs may include programs of ... related to clinical development. Coordinates and participates as the DS study owner in regulatory inspections and internal quality audits + Participates in… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and are responsible for the execution of RWE safety epidemiology studies across the product lifecycle, including pediatrics, post authorization studies ... Evidence (RWE) function at Gilead is part of the Clinical Data Sciences (CDS) group within the Development organization...track record in the design and conduct of epidemiologic studies , direct expertise in use of RWE and application… more
- Gilead Sciences, Inc. (Foster City, CA)
- …not limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical study endpoints, calculating sample ... capability development. **RESPONSIBILITIES:** + Acts as biostatistics lead on clinical studies or other non-molecule projects. +...projects and / or the statistical analysis plan and clinical study endpoints for assigned products. +… more
- Stanford University (Stanford, CA)
- … Research Coordinator Associate to perform duties related to the coordination of clinical studies . The CRCA will coordinate moderately complex aspects of one ... or more clinical studies . The CRCA will work under...close-out. + Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment… more
- Stanford University (Stanford, CA)
- …stakeholders-to support patients with heart failure. Responsibilities include providing clinical and administrative nursing support, administering study ... outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies . +...information (written and verbal). + Ability to implement good clinical practices in all interactions with study … more
- Gilead Sciences, Inc. (Foster City, CA)
- … research + Deep understanding of Phase I-IV clinical studies , clinical operations, and the roles of cross-functional study team members + Advanced ... design RBQM data flows to integrate with other relevant clinical and operational databases at study , program,...other relevant clinical and operational databases at study , program, and enterprise level. + Review central monitoring… more
- University of Southern California (Los Angeles, CA)
- … study sponsor. + Assists in participant recruitment for studies including recruitment, screening, orientation and correspondence. Schedules subject appointments, ... a lead coordinating aspects of sponsor-initiated and investigator-initiated research studies and D&I program including subject recruitment, data collection,… more
- System One (Walnut Creek, CA)
- …Clinical Principal Investigator (PI) provides medical leadership and overall oversight for clinical research studies conducted at various US based sites. This ... clinical research ethics. + Proven leadership in managing clinical teams and ensuring study compliance. + Excellent clinical judgment, organizational, and… more