- University of Pennsylvania (Philadelphia, PA)
- …patients, their caregivers, and others + Collaborate with call center team, supervisor , and principal investigators (eg, maintain study manuals of procedures, ... trackers, organize documentation, generate reports). + Assist with qualitative studies in partnership with members of the study team (eg, develop interview… more
- Stanford University (Stanford, CA)
- … studies . Work under supervision of the principal investigator and/or study coordinator/ supervisor . **Duties include*:** + Schedule and/or call subjects for ... + Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …collaborate with the DFCI Clinical Trials Office (CTO), the Office for Human Research Studies (OHRS), and the Office of Data Quality (ODQ) to fulfill local and ... and grant managers, may maintain, monitor and reconcile all study and related grant finances. These may include budget...guidelines for monitoring data quality control for PI Initiated studies / Multi-Center Trials * The CRM will oversee… more
- Stanford University (Stanford, CA)
- … studies . Work under supervision of the principal investigator and/or study coordinator/ supervisor . Duties include: + Schedule and/or call subjects for ... + Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
- Charles River Laboratories (Cleveland, OH)
- …drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies , and ... in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into … more
- Cedars-Sinai (Los Angeles, CA)
- …information; present this information at regular research staff meetings. + Notifies direct supervisor about concerns regarding data quality and study conduct. + ... research?** The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol… more
- NextEra Energy (Des Moines, IA)
- …and Transmission Owners (TO) to review and evaluate interconnection standards and study practices, transmission siting feasibility, system impact studies , and ... especially relating to baseline reliability planning and generator interconnection studies + Understanding of transmission policy and regulatory issues related… more
- Cedars-Sinai (Los Angeles, CA)
- …+ Schedules and participates in monitoring and auditing activities. + Notifies direct supervisor about concerns regarding data quality and study conduct. + Works ... The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility,… more
- University of Miami (Miami, FL)
- …procedures according to the protocol.2. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants.6. Addresses adverse events per protocol, advocating for study … more
- University of Miami (Miami, FL)
- …procedures according to the protocol. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. Addresses adverse events per protocol, advocating for study … more