Clinical Research Nurse I: Study Coordination & Care

The Medical College of Wisconsin, Inc.

Wauwatosa (WI)

On-site

USD 60,000 - 85,000

Full time

14 days+
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Benefits offered by this job

Health insurance
Dental insurance
Vacation and holidays
Tuition reimbursement
Parental leave
Retirement plan

Job summary

The Medical College of Wisconsin, Inc. is seeking a Clinical Research Coordinator to conduct clinical research studies, implement protocols, and document observations.

You will coordinate patient participation, enroll and consent patients, organize visits, and assist with data collection and regulatory submissions. Under physician direction, you will perform protocol-specific tasks, provide patient education, maintain records, and ensure compliance with IRB and regulatory requirements while

Qualifications

  • Knowledge of biology, chemistry, mathematics, documentation, and records management.
  • Data utilization, complex problem solving, critical thinking, resource management, and writing skills.

Responsibilities

  • Coordinate, evaluate and follow patient participation in clinical research.
  • Identify, enroll and consent patients; organize study visits and follow-ups.
  • Assist in data collection and monitoring; perform protocol-specific clinical tasks under physician direction.
  • Provide patient and family education; assist with IRB protocol submissions and grant applications.
  • Maintain patient records and confidentiality; enter data into databases; notify about complications.

Skills

Biology knowledge
Chemistry knowledge
Documentation
Data utilization
Critical thinking
Writing skills

Education

Associate’s degree

Tools

Database entry

Job description

The Medical College of Wisconsin, Inc. is seeking a Clinical Research Coordinator to conduct clinical research studies, implement protocols, and document observations.

You will coordinate patient participation, enroll and consent patients, organize visits, and assist with data collection and regulatory submissions. Under physician direction, you will perform protocol-specific tasks, provide patient education, maintain records, and ensure compliance with IRB and regulatory requirements while

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