- Stanford University (Stanford, CA)
- …The CRCA will support federal and non- federal clinical research studies including dermatological and investigative work in support of clinical trials, ... coordinate moderately complex aspects of one or more clinical studies and work under close direction of...close-out. + Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment… more
- Stanford University (Stanford, CA)
- …set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. He/she will ... work as part of a clinical trials research team...Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all… more
- Pfizer (South San Francisco, CA)
- …proof of mechanism (POM), early signs of efficacy (ESOE) and proof of concept (POC) studies in Oncology. You will work in close collaboration with the Global ... operations and the project team, to meet enrollment and study delivery timelines. You will also work ...+ Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study … more
- J&J Family of Companies (Irvine, CA)
- …Research Leader.** This position is located in Irvine, California and has a hybrid work schedule of 3 days a week on-site. At Johnson & Johnson, we believe ... across the organization. **Key Responsibilities:** In accordance with all applicable federal , state and local laws/regulations and Corporate Johnson & Johnson,… more
- J&J Family of Companies (Irvine, CA)
- …Company -sponsored postmarket studies ) and low complexity regulated studies (eg, Postapproval, Real-world evidence) including study budget assessment, ... and sharing appropriate interpretation of clinical evidence generated from research studies + Leading study -related publication efforts including abstracts,… more
- The County of Los Angeles (Los Angeles, CA)
- …with an opportunity for permanent County employment. Before the end of your initial work period, you will be assessed on your work performance. This assessment ... reports, survey results, focus group data, legislation, laws, County code, State/ Federal regulations) that serve justice impacted individuals. + Designs and… more
- Cedars-Sinai (Los Angeles, CA)
- …and leading staff. + Provides guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies . + May assist ... This is an **on-site role** with a **4/10 schedule** , offering a great work -life balance. If you hold an **active RN license in California** and have **prior… more
- Cedars-Sinai (Los Angeles, CA)
- …humankind?** The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol ... the informed consent process. Responsible for oversight of all studies with the group and the assignment of ...and identifying new research opportunities. Ensures compliance with all federal and local agencies including the Food and Drug… more
- Cedars-Sinai (Beverly Hills, CA)
- **Job Description** **This position offers a hybrid schedule, with the flexibility to work from home up to 2 days per week. However, candidates must reside in the ... II is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in medical monitoring and addressing medical concerns that arise during clinical studies , experience leading study concept and protocol design, and track-record ... innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking...active therapeutic area with phase 3 and 4 PBC studies and global regulatory filings underway or expected, with… more