Clinical Research Coordinator: Trials & Patient Care

Arizona Arthritis and Rheumatology Research, PLLC; Sun City (AZ); On-site; USD 45,000 - 65,000; Full time

Job summary

Arizona Arthritis & Rheumatology Associates, P.C. is seeking a Clinical Research Coordinator I to join our team.

The CRC coordinates and implements assigned protocols in compliance with FDA CFR, GCP and SOPs, collects data, assists in patient assessments, maintains study files and ensures accurate documentation and reporting. The ideal candidate has an Associate degree or equivalent, strong organizational and communication skills, and the ability to work with investigators and participants

Qualifications

• Associates Degree or equivalent required.
• Strong organizational and communication skills.
• Ability to develop professional relationships with providers and research subjects.
• Extensive knowledge of clinical research, ICH-GCP and regulations.
• Ability to lift up to 20 pounds.

Responsibilities

• Coordinate and implement assigned observational and clinical trials.
• Recruit and screen potential participants and review charts.
• Maintain study files and inventory; ensure accurate data entry.
• Ensure proper consent, adverse event reporting, and regulatory filings.
• Triages adverse events and coordinates with PI and monitors.
• Liaise with physicians, staff, and vendors; travel as needed.

Skills

Organizational skills

Communication skills

Professional relationship building

Knowledge of clinical research

Ability to lift 20 pounds

Education

Associate degree or equivalent

Job description

Arizona Arthritis & Rheumatology Associates, P.C. is seeking a Clinical Research Coordinator I to join our team.

The CRC coordinates and implements assigned protocols in compliance with FDA CFR, GCP and SOPs, collects data, assists in patient assessments, maintains study files and ensures accurate documentation and reporting. The ideal candidate has an Associate degree or equivalent, strong organizational and communication skills, and the ability to work with investigators and participants