Clinical Research Coordinator I
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![]() United States, Wisconsin, Milwaukee | |
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Summary Perform the day-to-day administrative activities of the clinical research trials program in Neurosciences. Provide support to the team to facilitate the achievement of the program's goals. Primary Responsibilities * Recruit, screen, enroll and obtain consent from program participants. 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 program data. Report program data and progress to program stakeholders. * Assist with study sample collection and processing. * 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. * Assist in the preparation of IRB documents and reports. Assist in the evaluation and writing of research protocols. * Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports. * Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program. * Maintain program timeline including tracking deadlines for program components. * Coordinate program outreach activities including acting as a liaison with community organizations. * Other duties as assigned. Knowledge - Skills - Abilities
Qualifications Appropriate experience may be substituted on equivalent basis. Minimum Required Education: Associate's Degree Minimum Required Experience: 1 year Required Certification/Licensure(s): CITI training within 90 days of hire #LI-NI1
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