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Clinical Research Coordinator I
Clinical Research Coordinator I-March 2024
Milwaukee
Mar 29, 2026
About Clinical Research Coordinator I

  JOB REQUIREMENTS: Position Description: Clinical Research Coordinator IPurpose Perform the day-to-day administrative activities of the clinicalresearch trials program. Provide support to the team to facilitate theachievement of the program\'s goals. Primary Functions Recruit, screen,enroll and obtain consent from program participants. Conduct orcoordinate training for program participants. Coordinate researchprotocols including arranging necessary appointments and procedures,working collaboratively with other departments and institutions, andmaintaining contact with study participants. Maintain patient calendars,screening and enrollment information utilizing the OnCore software toolto assist in patient specific protocol required timelines to ensurecompliance with protocol requirements. Monitor the study relatedactivities on a patient and protocol level. Collect, analyze, anddisseminate program data. Report program data and progress to programstakeholders. Identify problems or obstacles in the system/proceduresrelated to implementation of the research protocols and communicate tothe study investigators. Assure compliance with all relevant IRB andother regulatory agency requirements. Assist in the preparation of IRBdocuments and reports. Assist in the evaluation and writing of researchprotocols. Collaborate on the development of program materials includingeducational materials, marketing materials, websites, forms, andreports. Work with Principal Investigator to develop, implement, andmaintain comprehensive databases and files related to the program.Maintain program timeline including tracking deadlines for programcomponents. Coordinate program outreach activities including acting as aliaison with community organizations. Work with CTO Beacon Coordinator,and entire Beacon review team, to assist with protocol specific orderingsystem requirements to assure protocol compliance. Assist in thepreparation of IRB documents and reports. Facilitate monitoring andaudit related activities. Process and ship lab specimens as necessary.Knowledge - Skills - Abilities Knowledge of biology, chemistry,mathematics, documentation, and records management. Data utilization,complex problem solving, critical thinking, resource management, andwriting skills. Preferred Schedule: Fulltime 8-4:30 PositionRequirements: Specifications Appropriate experience may be substitutedfor education on an equivalent basis Minimum Required Education:Associate\'s Degree Minimum Required Experience: 1 year of experience inresearch. Preferred Education: Bachelors degree PreferredExperience:... For full info follow application link. EEO/AAMinorities/Females/Vets/Disability The Medical College of Wisconsin isan affirmative action/equal opportunity employer and does notdiscriminate in hiring or employment on the basis of age, sex, race,color, religion, national origin, veteran status, disability or sexualorientation. ***** APPLICATION INSTRUCTIONS: Apply Online:ipc.us/t/C057FF6FAC7541DD Qualified females, minorities, and specialdisabled veterans and other veterans are encouraged to apply.

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