- Cedars-Sinai (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
- AbbVie (San Francisco, CA)
- …+ Has overall responsibility for oversight of the Medical Affairs-led clinical studies , monitoring overall study integrity and review, interpretation and ... safety and efficacy of the molecule. As the SD Study Lead, is responsible for oversight of study... Study Lead, is responsible for oversight of study enrollment and overall timelines for key deliverables. +… more
- BeOne Medicines (San Mateo, CA)
- …and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts + Clinical sections of INDs ... areas for the successful implementation and execution of clinical studies + Provide scientific expertise for selection of investigator...data both internally and externally + Represent a clinical study or development program on one or more teams… more
- Cedars-Sinai (Beverly Hills, 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
- Cedars-Sinai (Los Angeles, CA)
- …Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. ... limited patient contact with research participants 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)
- …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
- 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
- Merck (Sacramento, CA)
- …approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The Regional Medical Scientific Director serves as a ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial… more
- Bristol Myers Squibb (San Diego, CA)
- …responsible for the design, implementation, monitoring, analysis, and reporting of studies conducted within RayzeBio's portfolio to ensure the program meets the ... and partner with investigators and CROs to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study… more
- City of Long Beach (Long Beach, CA)
- …of the annual budget; performs preliminary research, investigations, and studies ; develops preliminary interpretations and makes recommendations for improvement in ... or other identifying characteristic on the form. Degrees must indicate the field of study and transcripts must indicate the field of study and degree conferred… more