- CommonSpirit Health (Santa Maria, CA)
- …Institute. Duties may vary depending on the size and complexity of each study . This role assists with clinical trial or other research project coordination duties ... reporting, source documentation and research record development and maintenance; study drug accountability; specimen collection, processing and shipment. The… more
- CommonSpirit Health (Santa Maria, CA)
- …Research Institute. The incumbent has responsibility for the oversight of studies that explore complex medical diseases, which involve specialty and subspecialty ... injections, and other procedures appropriate within the RN scope of + Dispense study medication to research participants under the direction of the PI, and/or… more
- Cedars-Sinai (Beverly Hills, CA)
- …area.** The Clinical Research Coordinator II works independently providing study coordination including 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
- Stanford University (Stanford, CA)
- …+ Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews ... to gather data, as needed. + Administer standard study questionnaires and tests, score test measurements and questionnaires,...accuracy. + Extract data from source documents for research studies as directed. Collect data and complete case report… more
- Cedars-Sinai (Los Angeles, CA)
- …Research Program Administrator, or Research Nurse to coordinate and/or implement the study . This role evaluates and abstracts research data and ensures compliance ... 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
- Cedars-Sinai (Los Angeles, CA)
- …role?** The Clinical Research Coordinator II works independently providing study coordination including 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
- Cedars-Sinai (CA)
- …our team!** The Clinical Research Coordinator II works independently providing study coordination including 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)
- …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
- BeOne Medicines (Emeryville, CA)
- …+ Provide guidance to the CST and ensure timely, quality, and efficient study planning and execution of associated clinical programs/ studies + Conduct regular ... lead and manage the Global Clinical Program Lead (GCPL)/ Global Clinical Study Manager (gCSM) group in designated Franchise(s)- therapeutic area (s) or asset(s),… more
- Ventura County (Ventura, CA)
- …para-professional and technical duties or to assist with special projects or studies . Students are provided with practical experience in fields which may be ... related to their fields of study . PAYROLL TITLE: HCA Student Worker SALARY: $21.00/Hour AGENCY/DEPARTMENT:...information and conducting investigations. + Assists in conducting special studies in a variety of occupational fields. + May… more