- Stanford University (Stanford, CA)
- …study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to ... define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study… more
- Stanford University (Stanford, CA)
- …study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted to ... define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study… more
- Cedars-Sinai (Los Angeles, CA)
- …Operating Procedure development, etc. *May participate in the development of Investigator Initiated trials for Investigational New Drug applications and/or ... field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures,… more
- The County of Los Angeles (Los Angeles, CA)
- …Program Analyst . Option Ill: Three years of experience at the level of Investigator , Pretrial Services, Probation . Option IV: One year of experience at the level ... of Senior Investigator , Pretrial Services, Probation . License: A valid California...Own Recognizance, Pretrial Supervision, Electronic Monitoring, Early Disposition, or Drug Court. This class, under general supervision, interviews, investigates… more
- BeOne Medicines (San Mateo, CA)
- …and up to 2 studies in late development) + Seamless transition of drug candidates from research to early clinical development + Effective integration of in-licensed ... drug candidates into early clinical development portfolio + Effective...and other functional teams, as appropriate + Assessment of Investigator Initiated & Collaborator Research program **Essential Functions of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Document writing and review - Including but not limited to, protocols, investigator brochures, clinical study reports and other clinical trial documents + Conduct ... investigator meetings and lead site initiation visits with clinical...visits with clinical trial investigators + Implement and deploy drug development strategic plans and meet milestones + Translate… more
- Bristol Myers Squibb (San Diego, CA)
- …team. This position provides operational and scientific support of investigator -initiated trials, to ensure their successful implementation. This individual is ... several departments (Clinical Operations, CMC, Regulatory Affairs, Supply Chain, Drug Safety/PV, Compliance and Legal). **Responsibilities:** Essential duties and… more
- BeOne Medicines (San Mateo, CA)
- …concepts, synopses, protocols, and amendments o Informed consent documents; + Investigator Brochures o Clinical study reports; + Abstracts, posters and manuscripts ... Update Reports; + Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports; + Risks / benefits analysis for applicable… more
- BeOne Medicines (San Mateo, CA)
- …+ Protocol concepts, synopses, and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts + ... Update Reports + Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports + Risks / benefits analysis for applicable… more
- Cedars-Sinai (Los Angeles, CA)
- …Clinical Coordinating Center (CCC) offers infrastructure and expertise for investigator -initiated trials (IITs) and collaborative, multi-site clinical research. The ... internal and external stakeholders to coordinate all aspects of assigned investigator -initiated and multi-site projects. The Clinical Research Specialist II provides… more