Job Information
BLOODCENTER OF WISCONSIN, INC Senior Clinical Research Coordinator in MILWAUKEE, Wisconsin
JOB REQUIREMENTS: Senior Clinical Research Coordinator Job Locations US-WI-Wauwatosa ID 2024-10717 Category Research and Development Position Type Full Time Overview Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced 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 and helping our healthcare partners thrive. Position Summary Under the direction of the Principal Investigators (PIs) and CTRO Supervisor, is responsible for coordinating research trials from initiation to completion in compliance with regulations and requirements. Manages trial budgets and implements and oversees systems to manage the conduct of the clinical trials and the flow of information among stakeholders. May serve as a team lead or experienced coordinator mentor. May lead a disease function research area. Responsibilities Subject Interaction: * Obtains consent and enrolls study subjects. * Communicates with study subjects, ensuring they receive applicable information. May include training and education regarding the study. * Serves as a liaison between study subjects and Principal Investigator/research team to provide proactive communication. * May collect samples from subjects as applicable/assigned. Stakeholder Interaction: * Serves as a liaison with stakeholders including members of the research team, IRB (Institutional Review Board), study sponsors, hospitals/hospital staff, BCW staff, national data coordinating centers, and granting agencies. May include training and education regarding the study. * Ensures receipt of applicable study data, reports, contracts, and information. Administrative Responsibilities: * Coordinates the conduct of the clinical research project and protocols from initiation to completion in compliance with regulations and requirements. * Designs, oversees, evaluates, and improves systems and processes to manage... For full info follow application link. We embrace and encourage diversity in our workforce. Equal Opportunity Employer of Minorities, Females, Protected Veterans, and Individuals with Disabilities. We participate in eVerify. We maintain a drug-free workplace and perform pre-employment substance abuse testing. We are a tobacco/smoke-free workplace. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/66BBFA0C7D7E4142 Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.