- AbbVie (Irvine, CA)
- …meetings. *Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying ... markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff. *May have… 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 ... processing data, maintaining record systems, and producing project reports for studies . In addition, may train clinical research staff, perform basic statistical… more
- GRAIL (Menlo Park, CA)
- …we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to overcome one ... selection, start-up, enrollment, maintenance, and close-out + Prepares and reviews study related plans and documents including protocols, informed consent forms,… 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 thought leaders to design a clinical development plan for nominated drug candidates + Lead internal project teams, and partner with investigators and… more
- CommonSpirit Health (Santa Maria, CA)
- …to research participants under the direction of the PI, and/or coordinate study drug administration with hospital/clinic Pharmacy staff. + Process labs ... Institute. The incumbent has responsibility for the oversight of studies that explore complex medical diseases, which involve specialty...well as protocol deviations, violations or exceptions, to the study sponsor and IRB as required by GCP, FDA,… more
- BeOne Medicines (San Mateo, CA)
- …to apply their existing skills to oncology + Expert understanding of global clinical study design and drug development process from discovery to registration and ... and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts + Clinical sections of INDs… more
- Cedars-Sinai (Los Angeles, CA)
- …field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, ... Research Program Administrator, or Research Nurse to coordinate and/or implement the study . This role evaluates and abstracts research data and ensures compliance… 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...all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. +… 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...all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. *Maintains… more
- BeOne Medicines (Emeryville, CA)
- … and development programs. . Collaborate with Clinical Pharmacology to design studies involving PK, ADME, bioavailability, and drug - drug interactions. ... provide strategic statistical leadership for pharmacokinetic (PK) and pharmacodynamic (PD) studies across all phases of clinical development. This role partners… more
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