Clinical Research Coordinator II - REDCap & Neurology Trials

The University of Arizona

Phoenix (AZ)

On-site

USD 53,000 - 66,000

Full time

2 days ago
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Benefits offered by this job

Health, dental, and vision insurance
Life insurance and disability programs
Paid vacation, sick leave and holidays
Tuition reduction for employee and fam
State retirement plan
Access to UA recreation and cultural活动

Job summary

The University of Arizona College of Medicine - Phoenix invites applications for a Clinical Research Coordinator II in the Department of Neurology. Based at Banner University Medical Center-Phoenix, the CRC II will oversee daily operations, data management, and regulatory compliance for complex, multi-center trials.

Responsibilities include recruitment, study coordination, data handling, and collaboration with faculty and staff.

Qualifications

  • Bachelor's degree or equivalent advanced learning.
  • Three years of relevant work experience or an equivalent combination of education and experience.
  • Experience building REDCap study databases.

Responsibilities

  • Recruitment and enrollment: screen eligibility, obtain consent, educate participants and coordinate staff education.
  • Research coordination: administer treatments, monitor health, ensure protocol adherence and consent.
  • Data coordination: build REDCap databases, collect data, maintain records and ensure data quality.
  • Troubleshooting: coordinate with departments, plan enrollment strategies, manage study supplies.
  • Compliance and education: ensure regulatory compliance, complete human subjects training, ongoing professional development.

Skills

Multitasking
Communication
Stakeholder interaction
Independent judgment

Education

Bachelor's degree or equivalent

Tools

REDCap

Job description

The University of Arizona College of Medicine - Phoenix invites applications for a Clinical Research Coordinator II in the Department of Neurology. Based at Banner University Medical Center-Phoenix, the CRC II will oversee daily operations, data management, and regulatory compliance for complex, multi-center trials.

Responsibilities include recruitment, study coordination, data handling, and collaboration with faculty and staff.

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