Clinical Research Coordinator


Milwaukee, WI

What you'll be doing

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. 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 principle 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.

What your background should be

Minimum 2 years of experience in research program coordination. Experience with program management in a medical research or educational environment preferred. Prior work with clinical research or patient care preferred. Background in psychology preferred. Excellent oral and written communication skills are essential. Strong critical thinking, problem solving and attentiveness to detail required. Strong computer skills. Sufficient knowledge of the program study area.

Required Schooling / Training

BS or BA degree.

Who is the client company

This is a private, freestanding medical school and graduate school of sciences in the central United States.
If you are interested in this position, send your resume to