- Taiho Oncology (Pleasanton, CA)
- …of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting of clinical trials. Performance Objectives: + Collaborates ... the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs),...and leverages the knowledge for designing and summarizing clinical studies . + Keeps Sr. Medical Director current on status… more
- Cedars-Sinai (Los Angeles, CA)
- …Description** 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
- BeOne Medicines (San Mateo, CA)
- …internal governance committees + Provides leadership and clinical oversight across all assigned studies and programs (up to 2 programs in early development and up to ... 2 studies in late development) + Seamless transition of drug...+ Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts + Clinical… more
- US Tech Solutions (South San Francisco, CA)
- …Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining ... and PI, is responsible for independently conducting clinical research sessions with study participants. + These sessions will be conducted on-site in South San… more
- Merck (Sacramento, CA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial… more
- Cedars-Sinai (Los Angeles, CA)
- …Clinical Research Data Associate II manages the data for assigned research studies . This will include, designing forms for data collection, clinical data ... data, maintaining record systems, and producing project reports for studies . In addition, may train clinical research staff, perform...required training and education programs. + Works closely with study monitors to review study data and… more
- Bristol Myers Squibb (San Diego, CA)
- …the internal and external network + Manages Phase 1 - Phase 4 studies , with demonstrated decision making capabilities + Provides medical and scientific expertise to ... and is a key member of a high performing Study Delivery Team (SDT) and may be a member...Provides oversight and medical accountability for a group of studies + Leads the analysis of benefit/risk for clinical… more
- BeOne Medicines (San Carlos, CA)
- …Clinical Biomarker Scientist to lead biomarker strategy and execution in clinical studies . The role involves designing and analyzing biomarker studies , ... the job:** + Serve as the primary biomarker scientist for the clinical study team, ensuring biomarker strategies are integrated into clinical development plans. +… more
- Terumo Neuro (Aliso Viejo, CA)
- …Description:** The Senior Manager, CDM oversees clinical data management activities across multiple studies from study start-up through study closure. This ... validation specifications, data transfer agreements and data management plans. + Review study documents, eg clinical study protocols, statistical analysis plans,… more
- Terumo Neuro (Aliso Viejo, CA)
- …on project teams, assist in the implementation of controlled clinical studies of MicroVention products. + Understand, read, and prepare technical documentation ... including, informed consents, study forms, and study training documents. +...+ Work closely with Project Manager(s) to ensure clinical studies are conducted in accordance with the protocol, GCP,… more