JOB REQUIREMENTS: Clinical Research Coordinator Job LocationsUS-WI-Wauwatosa ID 2024-9404 Category Research and Development PositionType Full Time Overview Versiti is a fusion of donors, scientificcuriosity, and precision medicine that recognize the gifts of blood andlife are precious. We are home to the world-renowned Blood ResearchInstitute, we enable life saving gifts from our donors, and provide thescience behind the medicine through our diagnostic laboratories. Versitibrings together outstanding minds with unparalleled experience intransfusion medicine, transplantation, stem cells and cellulartherapies, oncology and genomics, diagnostic lab services, and medicaland scientific expertise. This combination of skill and knowledgeresults in improved patient outcomes, higher quality services andreduced cost of care for hospitals, blood centers, hospital systems,research and educational institutions, and other health care providers.At Versiti, we are passionate about improving the lives of patients andhelping our healthcare partners thrive. Position Summary Under thedirection of the Principal Investigators (PIs) and CTRO Supervisor, isresponsible for coordinating research trials from initiation tocompletion in compliance with regulations and requirements. Assists inthe management of trial budgets and implements and oversees systems tomanage the conduct of the clinical trials and the flow of informationamong stakeholders. Responsibilities Subject Interaction: * Obtainsconsent and enrolls study subjects * Communicates with study subjects,ensuring they receive applicable information. May include training andeducation regarding the study * Serves as a liaison between studysubjects and Principal Investigator/research team to provide proactivecommunication * May collect samples from subjects asapplicable/assigned Stakeholder Interaction: * Serves as a liaison withstakeholders including members of the research team, IRB (InstitutionalReview Board), study sponsors, hospitals/hospital staff, BCW staff,national data coordinating centers, and granting agencies. May includetraining and education regarding the study * Ensures receipt ofapplicable study data, reports, contracts, and informationAdministrative Responsibilities: * Coordinates the conduct of theclinical research project and protocols from initiation to completion incompliance with regulations and requirements * Designs, oversees,evaluates, and improves systems and processes to manage the conduct ofthe clinical trial and the flow of information among stakeholders *Prepares a... For full info follow application link. We embrace andencourage diversity in our workforce. Equal Opportunity Employer ofMinorities, Females, Protected Veterans, and Individuals withDisabilities. We participate in eVerify. We maintain a drug-freeworkplace and perform pre-employment substance abuse testing. We are atobacco/smoke-free workplace. ***** APPLICATION INSTRUCTIONS: ApplyOnline: ipc.us/t/D9106186DC604CAB Qualified females, minorities, andspecial disabled veterans and other veterans are encouraged to apply.