JOB REQUIREMENTS: Position Description: Clinical Research Coordinator II - GOOD Study Purpose Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the team to facilitate the achievement of the program\'s goals. Assist with recruiting, training, and supervising staff and managing the program budget. Primary Functions * Recruit, screen, enroll and obtain consent from program participants GOOD Study randomized control trial, data registry, and biobank. Conduct or coordinate training for program participants. * Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants. * Collect, analyze, and disseminate research data. Report program data and progress to study investigators and program stakeholders including DSMB, GOOD Study Steering and Subspecialty Committees, division/department/organizational leadership, external sponsors, regulatory bodies, and collaborators. Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program. * Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators. * Assure compliance with all relevant IRB and other regulatory agency requirements. * Prepare IRB documents and reports to the NIH. Evaluate and write of research protocols in collaboration with the study investigator. * Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports. Maintain and update GOOD Study Clinicaltrials.gov page(s). Assist in maintenance of GOOD Study webpage, as needed. * Maintain program timeline including tracking deadlines for program components. * Coordinate program outreach activities including acting as a liaison for the 38 participating sites. Organize internal and external meetings, site visits, and special events. * Monitor study related budgets. Participate in the development of program resources through literature searches, contact with outside programs, and review of funding opportunities. Knowledge - Skills - Abilities Knowledge of biology, chemistry, mathematics, documentation, and records management. Data utilization, complex problem solving, critical thinking, resource management, and writing skills. Preferred Schedule: Position Requirements: Specifications Appropriate experience may be substituted for education on an equivalent basis Minimum... For full info follow application link. EEO/AA Minorities/Females/Vets/Disability The Medical College of Wisconsin is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, veteran status, disability or sexual orientation. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/284E5D4A046548CD Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.