Clinical Research Coordinator I/II – Orthopedics
University of Wisconsin-Madison
full-time
Posted on:
Location Type: Hybrid
Location: Madison • Wisconsin • United States
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Salary
💰 $49,000 - $55,000 per year
Job Level
About the role
- support a growing and dynamic clinical research portfolio
- collaborate with nationally recognized investigators and multidisciplinary teams
- assist with manuscript preparation, authorship activities, and grant development
- coordinate multiple ongoing, multi-center clinical trials
- manage research workflow components and collect participant data
- recruit, screen, select, determine eligibility and enroll trial participants
Requirements
- 0-2 years of clinical research experience, including experience with human subjects research
- Prior experience adhering to IRB approved protocols
- Prior experience with data entry
- Prior experience with electronic medical/health records (EMR or EHR) systems
- Schedule flexibility preferred
- 2 years of clinical research experience, including experience with human subjects research
- Prior experience consenting and enrolling human subjects
- Prior experience adhering to IRB approved protocols
- Prior experience with FDA regulated clinical trials
- Prior experience with electronic data capturing (EDC) systems
- Prior experience with Clinical Trial Management Systems (CTMS)
- Prior experience managing multiple research projects simultaneously
- Prior experience with monitoring audits both internal and external
- Bachelors Degree preferred; focus in biology, chemistry, kinesiology, biomedical engineering, or other related fields preferred.
Benefits
- generous vacation, holidays, and sick leave
- competitive insurances and savings accounts
- retirement benefits
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical research experiencehuman subjects researchdata entryelectronic medical recordselectronic health recordselectronic data capturingClinical Trial Management SystemsFDA regulated clinical trialsmanaging multiple research projectsmonitoring audits
Soft Skills
collaborationcommunicationorganizationflexibility