- IQVIA (Carlsbad, CA)
- …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines of communication with… 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
- 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...Category** : Academic / Research **Job Specialty** : Research Studies / Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift**… more
- Stanford University (Stanford, CA)
- …more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies . ... sponsor meetings, and team communications. + Oversee subject recruitment and study enrollment goals; develop and implement effective strategies for participant… more
- Cedars-Sinai (Los Angeles, CA)
- …Children's. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… 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
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, ... queries. This role is responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other… more
- Cedars-Sinai (Los Angeles, CA)
- …to assist in tasks supporting the coordination/implementation of noncomplex research studies . Supports objectives of research studies through noncomplex tasks ... to assist in tasks supporting the coordination/implementation of noncomplex research studies . + Collects, evaluates and/or abstracts clinical research data. May… more
- Merck (South San Francisco, CA)
- …determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and ... drugs. + Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as...and efficacy as well as new drug applications, clinical study reports, or publication; and + Participation in internal… more
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