JOB REQUIREMENTS: Position Description: Position Summary Position: Clinical Research Coordinator II Purpose Perform the day-to-day administrative activities of Clinical Trial\'s Office (CTO) for the Department of Medicine (DOM). Work closely with team and leadership on trial management. Provide support to the team to facilitate the achievement of the DOM CTO\'s goals. Assist with trial management, onboarding, and training of research staff, faculty, and learners. Primary Functions Conduct or coordinate training for program participants. Collect, analyze, and disseminate research data. Report study related data and progress to study to management, study investigators, and sponsors are required. 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 and study team. Conduct and coordinate training for investigative team. Prepare and submit IRB documents and reports. Assure compliance with all relevant IRB and other regulatory agency requirements. Monitor study related activities on a patient, protocol and financial level including budget negotiations. Collaborate on the development of Department processes and documentation including educational materials, marketing materials, websites, forms, and reports. Maintain timelines including tracking deadlines for individual research projects. Participate in the development of CTO resources through literature searches, contact with outside programs, and review of funding opportunities. Facilitate monitoring and audit related activities. Assist with study start-up and with multi-site trials. Process and ship lab specimens, as necessary. Recruit, screen, enroll and obtain consent from program participants. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments, ancillary partners and institutions, and maintaining contact with study participants. Maintain patient calendars, screening and enrollment information while utilizing the OnCore and Florence software tool to assist in patient specific protocol required timelines to ensure compliance with protocol requirements. Preferred Schedule: Full-time role with expectations for coverage during core business hours and flexibility required as necessary to accommodate business needs. Position Requirements: Knowledge - Skills - Abilities Experience in research or study coordination and/or compliance. Knowledgeable of... 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/B62934F511E44866 Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.