Clinical Research Coordinator II — Study Coordination & Data

UNIVERSITY OF ARIZONA; Phoenix (AZ); On-site; USD 53,039 - 66,299; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Tuition reduction

Job summary

The University of Arizona in Phoenix seeks a Clinical Research Coordinator II to support internal medicine clinical studies. You will coordinate enrollment, consent, data collection, and protocol adherence under supervision, interacting with faculty and staff across research activities.

Responsibilities include data management, regulatory compliance, and daily operations. Intermittent off-campus visits may be required; benefits are extensive and include health plans and tuition reductions.

Qualifications

• Bachelor's degree or equivalent advanced learning attained through professional level experience required.
• Three (3) years of relevant work experience, or equivalent combination of education and work experience.
• Phlebotomy certified.
• Excellent written and verbal communication skills; ability to interact with diverse stakeholders.

Responsibilities

• Recruitment and enrollment activities including eligibility screening, consent, and education materials.
• Coordinate clinical research operations, protocol adherence, and staff education across the clinic/hospital.
• Data collection, entry, and quality checks; prepare data for internal and external systems.
• Troubleshooting with other departments to ensure progress of study procedures and enrollment.
• Ensure compliance with federal regulations for human subjects research and sponsor expectations; support staff training.

Skills

Phlebotomy certified

multitask

communication skills

independent judgment

Education

Bachelor's degree

3 years of relevant experience

Job description

The University of Arizona in Phoenix seeks a Clinical Research Coordinator II to support internal medicine clinical studies. You will coordinate enrollment, consent, data collection, and protocol adherence under supervision, interacting with faculty and staff across research activities.

Responsibilities include data management, regulatory compliance, and daily operations. Intermittent off-campus visits may be required; benefits are extensive and include health plans and tuition reductions.