- Charles River Laboratories (San Diego County, CA)
- …finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel ... regular clinical rounds and routine health monitoring and examinations in support of studies and in accordance with the requirements of the research program, and… more
- Charles River Laboratories (South San Francisco, CA)
- …finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel ... regular clinical rounds and routine health monitoring and examinations in support of studies and in accordance with the requirements of the research program, and… more
- IQVIA (Carlsbad, CA)
- …monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study protocol, ... monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International… more
- Cedars-Sinai (Los Angeles, CA)
- …a part of breakthrough research?** The Clinical Research Associate I will work directly with a Clinical Research Coordinator, Research Program Administrator, or ... Research Nurse to coordinate and/or implement the study . Evaluates and abstracts research data and ensures compliance with protocol and research objectives.… more
- University of Southern California (San Diego, CA)
- …with research teams and community partners to ensure outreach efforts engage the study populations of interest and align with ATRI's mission to advance Alzheimer's ... and related dementias research through equitable study participation. Key Responsibilities: + Develop and execute outreach strategies that promote representative… more
- J&J Family of Companies (Irvine, CA)
- …manage company sponsored clinical trials, ensuring compliance with timelines and study milestones. + Oversees/executes feasibility, selection, set up, conduct and ... trial sites (eg site management); + Develops clinical trial documents (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator… more
- Stanford University (Stanford, CA)
- …according to study protocol + Contact and schedule participants for research studies and serve as primary contact from study start-up to closeout + ... school positions. **Duties Include:** + Assist in regulatory document preparation for study + Assist with the screening, recruiting, and gathering consent from … more
- Stanford University (Stanford, CA)
- …passionate about clinical research and wants to deliver results. The ACRC will work with a robust clinical research team, hand in hand with Principal Investigators, ... + Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
- 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 ... document review and data inclusion for NDA submissions of assigned studies by collaborating with cross-functional partners to meet clinical development project… more
- Gilead Sciences, Inc. (Foster City, CA)
- …approaches to optimize study parameters and interpret outcomes. + Prepare study protocols and coordinate execution of nonclinical studies which may involve ... innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking...include designing and interpreting in vitro and in vivo studies , integrating data into mathematical models, and generating simulations… more