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Milwaukee, WI; Froedtert Hospital Pavilion
Source: Medical College of Wisconsin careers · View original posting
From Medical College of Wisconsin's posting. “We” and “our” refer to the employer.
Summary
Perform the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program’s goals.
Primary Responsibilities
Working with multiple Principal Investigators ensure proper conduct of assigned Clinical Trials Office trials, Children’s Hospital of Wisconsin. Maintain regular contact and provide updates whenever necessary
Work closely with CTO leads/managers on a day-to-day basis providing updates and managing priorities.
Screen, recruit, enroll and obtain consent from study 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 study data. Report data and progress to PIs and CTSI 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, HIPAA, GCP and other regulatory requirements. Responsible for maintaining ongoing training, certifications and compliance with current regulations at MCW, CHW and VA.
Assist in the preparation of IRB documents and reports. Assist in the evaluation and writing of research protocols.
Collaborate on the development of study 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.
Process and ship lab specimens as necessary. IATA certification to be obtained within 30 days of hire.
Familiarity with EMR (EPIC) preferred.
Display familiarity in utilization of clinical trial management systems, proficiency with OnCore preferred.
Knowledge – Skills – Abilities
Knowledge of biology, chemistry, mathematics, documentation, and records management.
Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
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