- Johns Hopkins University (Baltimore, MD)
- …Research Coordinator II oversees the administrative and scientific implementation of clinical protocol for a complex* and/or multiple research studies. As part of ... with PI and study team to ensure operational feasibility of proposed protocol /study design. + Develop standard operating procedures and data collection forms from… more
- University of Miami (Miami, FL)
- …ancillary committees, study team, business office, and sponsors. Completion of the new protocol submission packet with the information provided by PRMC as well as ... any additional required documentation (ie local protocol , HIPAA forms, etc.). Modifying and standardizing consent forms...prepare the following forms for IRB submission to ensure protocol compliance with federal regulations. This process will take… more
- Houston Methodist (Houston, TX)
- …This position implements clinical research patient care via the research protocol . The CRN position works with the Performance Improvement department, sponsor, ... and coordinates with interprofessional team as written in the research protocol . Contributes to teamwork by consistently responding positively to requests for… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of study data into clinical trials management software, screening for protocol eligibility, and obtaining consent from patients for industry-sponsored and biobanking ... information. The CRC will ensure prompt collection and shipment of protocol -related samples to external entities as necessary. Responsible for maintaining regulatory… more
- University of Pennsylvania (Philadelphia, PA)
- …visits and with other divisions and/or service centers as required by the protocol . Arranging transportation to and from study visits + Prepare patient and ... appointments, procedures, or inpatient stays as required by study protocol + Perform specific protocol procedures such...required by study protocol + Perform specific protocol procedures such as interviewing subjects, taking vital signs,… more
- Cedars-Sinai (Beverly Hills, CA)
- …independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and ... for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study… more
- Cedars-Sinai (Los Angeles, CA)
- …independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and ... for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study… more
- Mount Sinai Health System (New York, NY)
- …collection and management of patient clinical information, timely collection of protocol related samples including shipment to outside entities as required, obtain ... + Coordinate research team to ensure compliance with planned treatment protocol including required laboratory and radiographic testing. + Secure, deliver, and… more
- Cleveland Clinic (Cleveland, OH)
- …and conduct of research projects ensuring adherence to research protocol requirements including **:** timely completion and communication of regulatory ... study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions. + Utilizes the nursing process… more
- Cedars-Sinai (CA)
- …providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating ... compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents… more