Clinical Trials Data Coordinator

Arizona Arthritis; Paradise Valley (AZ); On-site; USD 42,000 - 70,000; Full time

Job summary

Arizona Arthritis seeks a Clinical Research Assistant in Paradise Valley to support patient recruitment, data collection and trial coordination. The role involves daily patient interaction, consent processes and data entry for multiple trials.

Responsibilities include screening and enrolling patients, documenting adverse events, and ensuring protocol compliance with nurses, coordinators, and the Director of Research.

Qualifications

• Assess eligibility and enroll patients per study protocol.
• Verify eligibility criteria with medical records and PI/nurse.
• Explain informed consent and document adverse events.
• Extract data for CRFs from hospital/outpatient records.

Responsibilities

• Recruit and enroll patients into clinical trials per protocol.
• Discuss informed consent with patients and document processes.
• Monitor protocol adherence with clinicians and staff.
• Extract protocol data from records for CRF completion.

Skills

Eligibility assessment

Patient recruitment

Informed consent

Data extraction

Protocol compliance

Education

Bachelor's Degree in biological or health sciences

Tools

CGM LabDaq LIS

AllScripts

Paycom

MS Office

Job description

Arizona Arthritis seeks a Clinical Research Assistant in Paradise Valley to support patient recruitment, data collection and trial coordination. The role involves daily patient interaction, consent processes and data entry for multiple trials.

Responsibilities include screening and enrolling patients, documenting adverse events, and ensuring protocol compliance with nurses, coordinators, and the Director of Research.