- 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
- 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
- Stanford Health Care (Palo Alto, CA)
- …Evoked Potentials, Long-Term Monitoring in Epilepsy (LTME), Intraoperative Neurophysiologic studies , Nerve Conduction Velocity (NCV), and Tran cranial Doppler (TCD) ... studies . **Locations** Stanford Health Care **What you will do**...Technologist - CNCT (AANEM) or + Registered Nerve Conduction Study Technologist - R.NCS.T. (AAET) or + Certification for… more
- AbbVie (Irvine, CA)
- …clinical studies and ensures scientific integrity and interpretation of study data from a clinical development program. Provides medical and/or scientific ... direction to project/ study teams. Should expect to be asked to participate...etc.) as they relate to planned and on-going clinical studies or projects. + Assists in scientific education of… more