- Stanford University (Stanford, CA)
- …clinical studies . Coordinate moderately complex aspects of one or more clinical studies . Work under close direction of the principal investigator and/or ... study coordinator/supervisor. At Stanford University School of Medicine, the work we do touches the lives of those today and tomorrow. Through education,… more
- Parexel (Sacramento, CA)
- …operational performance data and presenting as an integral member of the Clinical Study team for clinical development studies . The reviews include interpretation ... data/trends and issues to be interpreted, reported and presented to the study teams. The Manager, Central Monitoring, will be responsible for supporting several… more
- Stanford University (Stanford, CA)
- …inspect study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted ... Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex projects/assignments. Independently manage… more
- Stanford University (Stanford, CA)
- …inspect study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted ... projects. The CRC2 will be instrumental in overseeing research studies primarily focused on pain and pain management in...coordinator will be responsible for managing data related to study outcomes, ensuring that all source documents are complete… more
- Cedars-Sinai (Beverly Hills, CA)
- **Job Description** **This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work ... onsite, 2 days remote. Standard hours 8:00am - 4:30pm. No expectation around weekend work . The expectation of this hybrid position is a minimum of 3days on campus,… more
- Stanford University (Stanford, CA)
- …studies . The CRCA will coordinate moderately complex aspects of one or more clinical studies . The CRCA will work under close direction of the Division Chief. ... primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility of and… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- … study questions from clinical trial sites in adherence to ICH GCP and the study protocol. + May lead less complex studies and/or manage components of more ... complex studies as a member of the study team + May participate in department initiatives or...a plus + Multiple years of experience managing the work of external candidates + Must be willing to… more
- Stanford University (Stanford, CA)
- …inspect study document to ensure ongoing regulatory compliance. + Work with principal investigator to ensure Investigational New Drug applications are submitted ... integral component of the Stanford Cancer Institute. The vital work performed there enables our adult and pediatric cancer...Independently manage significant and key aspects of a large study or all aspects of one or more small… more
- Merck (South San Francisco, CA)
- …guiding projects from late-stage preclinical work through clinical proof-of-concept studies . + **Translational study design** : Design, oversee, and ... of novel PET radiotracers from late preclinical development into first-in-human studies . This role will primarily focus on clinical implementation of novel… 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