- Rush University Medical Center (Chicago, IL)
- …research teams. Under close supervision, the CRA assists with essential study tasks such as organizing regulatory files, entering participant information, preparing ... materials for study visits, and observing study procedures for...for training. This role supports minimal to moderate risk studies , including exempt or expedited protocols, and is not… more
- AbbVie (North Chicago, IL)
- …markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and AbbVie study staff. + Has ... overall responsibility for leading clinical study teams, monitoring overall study integrity, and...for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying… more
- Stanford University (Stanford, CA)
- …more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies . ... sponsor meetings, and team communications. + Oversee subject recruitment and study enrollment goals; develop and implement effective strategies for participant… more
- University of Pennsylvania (Philadelphia, PA)
- …seeking a motivated Clinical Research Coordinator (CRC) to support research studies involving electroconvulsive therapy (ECT) for severe psychiatric illness. You ... treatment sessions. You will also help manage IRB protocols, maintain study documentation, and prepare data for manuscripts, grant proposals, and presentations.… more
- Sanofi Group (Morristown, NJ)
- …Director (CRD) and/or clinical lead in the medical/scientific contribution for the clinical studies on activities pertaining to the Study Medical Manager (SMM) ... responsibilities eg: leading or contributing to key study documents and activities from clinical development plans and...from clinical development plans and trial set-up to clinical study report in compliance with quality and regulatory processes.… more
- Hartford HealthCare (Hartford, CT)
- …of daily clinical trial activities and plays a critical role in the conduct studies . *This position will support a National Institutes of Health (NIH) funded ... study called, Exercise Values of Life & Vitality Everyday...Vitality Everyday (Evolve).* *Job Responsibilities:* * Maintains documentation of study training as needed. * Supports research projects in… more
- Cedars-Sinai (Los Angeles, CA)
- …Children's. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- University of Rochester (Rochester, NY)
- …and conduct human subject research, including receiving, distributing and explaining study information, such as protocol and human subject recruitment materials, to ... the protocol, including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form (CRFs) completion… more
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, ... queries. This role is responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other… more
- J&J Family of Companies (Irvine, CA)
- …work a Flex/Hybrid schedule with 3 days per week(could be more based on study support) onsite in our_ **_Irvine, CA office_** **.** **Purpose:** The Biosense Webster ... research and VOC analysis, User Performance evaluations eg EMG studies , formative and summative studies . The Senior...evaluations eg EMG studies , formative and summative studies . The Senior Human Factors Engineer has strong experience… more