- Genentech (South San Francisco, CA)
- …unit Clinical Operations DA level workgroups (eg, iCOP team), Clinical Operations leaders, project/ study teams, lifecycle teams to understand business ... site selection at DA level in addition to for study teams and ECD Clinical Operations management....expedite evidence generation and to accelerate the delivery of studies and product launches. * Utilizes state-of-art methodologies (including… more
- Medtronic (Los Angeles, CA)
- …with respect to the clinical , economic, and outcomes data from clinical trials and Real-World Evidence (RWE) studies including, epidemiology studies ... support on the design, execution, and dissemination of HEOR studies to meet the business needs. In this role,...on patient care. Responsibilities may include providing input on clinical trial design and Real-World Evidence (RWE) generation and… more
- Sleep Data (San Diego, CA)
- …The Sleep Technologist is responsible for preparing and conducting sleep studies in accordance with established protocols, including verifying medical orders, ... patient experience, with every patient interaction. + Prepare for sleep studies by reviewing patient history, verifying medical orders, and following established… more
- Cedars-Sinai (Beverly Hills, CA)
- …in providing direct patient nursing care within the context of supporting clinical trial study implementation. Works collaboratively with the Principal ... clinical education services to research participants and families regarding study participation, participant's current clinical condition, and or disease… more
- Kelly Services (Irvine, CA)
- …the Clinical R&D Department to support + execution of company sponsored clinical trials, ensuring compliance with timelines and study + milestones. + ... + Standard Operating Procedures + Contribute towards development of clinical trial documents (eg study protocol, informed...towards development of clinical trial documents (eg study protocol, informed + consents, CRF, monitoring plan, … more
- UCLA Health (Los Angeles, CA)
- …is seeking a Research Project Assistant to support the operational management of clinical research studies from design and start-up through completion and ... for implementing and coordinating research activities across one or more studies , ensuring compliance with study protocols, institutional policies, FDA… more
- Edwards Lifesciences (Irvine, CA)
- …methods and interpretation of results and also advise on the conduct of clinical studies , database development and data quality assurance with the analysis ... one or more clinical trials, lead the coordination of analyses for study report and other documents and provide programming and validation support of these… more
- Sumitomo Pharma (Sacramento, CA)
- …Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and ... inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable functions follow the requirements of the TMF… more
- Edwards Lifesciences (Irvine, CA)
- …unmet needs, overcome market access barriers, and drive impactful evidence for clinical , regulatory, and commercial success. This role also includes direct people ... execution, and delivery of multiple, concurrent RWE projects: including studies conducted internally and with external consultants-ensuring scientific rigor and… more
- Abbott (Sylmar, CA)
- …typically acquired in a recognized four-year or more academic course of study . Demonstrates aspects of technical or organizational leadership within the current ... projects. Has the ability to apply technical, clinical and marketing understanding of issues to bring tasks to resolution within assigned projects. Applies… more