- University of Colorado (Aurora, CO)
- …with patients expressing an interest and all pre-screening/screening activities. + Complete regulatory maintenance of assigned clinical trials (IRB and ... **Job Summary:** Key Responsibilities: + Act as a Primary Coordinator on multiple trials /studies, managing the day-to-day...study interviews. + Responsible for data management for all clinical trial data. Collect, code, and analyze… more
- Sanford Health (Sioux Falls, SD)
- …other personnel about the research process. Organize complex components of various clinical trials , including the coordination of study-required testing and ... in sponsor monitoring visits and audits to ensure compliance with regulatory requirements governing clinical research. Meet with monitors/auditors during… more
- University of Michigan (Ann Arbor, MI)
- …to hire a coordinator with expertise in conducting pharmaceutical-funded clinical trials . Participant Screening and Recruitment + Explaining study ... first day + 2:1 Match on retirement savings **Responsibilities Clinical Coordinator Responsibilities The position is looking...+ Facilitate Independent Monitoring Committee meetings + Add new clinical trials and update existing clinical… more
- Dignity Health (Phoenix, AZ)
- …The Ivy Brain Tumor Center at Barrow, is home to the largest Phase 0 clinical trials program in the world. Highly regarded for neuroscience education for ... systems. + Maintains records and insures compliance with applicable regulatory agency + Makes travel arrangements, schedules appointments, meetings, conferences… more
- University of Miami (Miami, FL)
- …of study coordinator service lines for CTRS/ MSOM investigators, encompassing regulatory and study management services for clinical research trials . ... Clinical Research (A) oversees the development of clinical trials and research programs that support...+ Prepares and presents the annual summary report for clinical trial and research areas. + Provides… more
- Houston Methodist (Houston, TX)
- …event reports, safety reports, and notifies IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory ... cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines *Assists with clinical trial budgets. *Schedules research participants for research visits and ... The Clinical Research Associate II works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse, or… more
- Covenant Health Inc. (Knoxville, TN)
- … clinical trials and human participant protection. In addition, the Clinical Research Nurse Coordinator assures compliance with protocol and regulatory ... clinical practices in the conduct of oncology clinical trials by possessing in-depth knowledge of...implements pre-study activities by developing timelines for conducting the clinical trial protocol, attending and participating in… more
- Cedars-Sinai (Los Angeles, CA)
- …(CRFs) + Assists with prescreening of potential research participants for various clinical trials . Schedules research participants for research visits and ... and Safety Letters in accordance with local and federal guidelines + Assists with clinical trial budgets and patient research billing + Responsible for sample… more
- Dana-Farber Cancer Institute (Boston, MA)
- …+ Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials. + Serves ... protocols. Research: + Assists with recruitment and registration of patients to clinical trials . + Coordinates scheduling of patient's laboratory and… more