Clinical Research Coordinator I - Emergency Medicine
On-siteMilwaukee, Wisconsin, United States
Job Summary
Recruit, screen, enroll, and obtain consent from program participants while conducting or coordinating training. Coordinate research protocols, arrange appointments and procedures, and maintain contact with study participants. Collect, analyze, and disseminate program data, then report progress to stakeholders. Identify system obstacles related to protocol implementation and communicate findings to investigators. Assure compliance with IRB and regulatory requirements, assist in preparing IRB documents, and help evaluate and write research protocols. Collaborate on developing program materials, databases, and files, and maintain program timelines including tracking deadlines. Coordinate outreach activities and act as a liaison with community organizations. Requires an Associate's Degree, one year of experience, and CITI training within 90 days of hire.
Required Qualifications
- Associate's Degree
- 1 year experience
- CITI training within 90 days of hire
- Knowledge of biology
- Knowledge of chemistry
- Knowledge of mathematics
- Knowledge of documentation
- Knowledge of records management
- Data utilization
- Complex problem solving
- Critical thinking
- Resource management
- Writing skills
- Ability to detect and translate speech or other communication
- Ability to distinguish colors
- Ability to perceive relative distances between objects
- Occasional lifting of moderate weight materials
- Ability to stand continuously
- Ability to walk continuously
- Occasional exposure to dust
- Occasional exposure to noise
- Occasional exposure to temperature changes
- Occasional contact with water or other liquids
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