- Valent BioSciences (San Ramon, CA)
- …guidelines, including study design and protocol development. Physical Demands and Work Environment (FIELD Position) The physical demands and work environment ... the quality of life for their customers. The corporate motto, Products That Work , From People Who Care(R), describes the company's business philosophy. Valent seeks… more
- Parexel (Sacramento, CA)
- …scientific questions, provide daily medical support to Parexel staff or site (investigator/ study coordinator), as needed + Review and sign off adverse events report ... for accuracy and clinical importance, relationship to the study drug as well as for severity and seriousness; provide sponsors with periodic experience reports… more
- Sumitomo Pharma (Sacramento, CA)
- …ensures accountable functions follow the requirements of the TMF SOP and system work instructions. Provide support and guidance to study team members during ... (TMF) Specialist will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs)...the full lifecycle of the study , including planning, set-up, maintenance, QC and closure of… 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...professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest… 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 (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...Proficiency in Word, PowerPoint and Excel. + Ability to work independently, set priorities, and handle multiple tasks requiring… 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, ... sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data,...professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest… more
- UCLA Health (Santa Monica, CA)
- …plays a critical role in the overall operational management of clinical research/trial/ study activities from design, set up, conduct, through closeout. The ideal ... responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored),… more
- Stanford University (Stanford, CA)
- …inspect study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted ... Wu Tsai Human Performance Alliance's Human Performance Lab and an ongoing, large-scale study to screen athletes for risk of anterior cruciate ligament injury. This… more
- Stanford University (Stanford, CA)
- …and administrative requirements to support the clinical trial operations for several research studies . This position will be involved in a range of duties including ... signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol. * Schedule and/or call subjects for… more