Rheumatology Clinical Research Coordinator

Arizona Arthritis and Rheumatology; Sun City (AZ); On-site; USD 52,000 - 72,000; Full time

Job summary

Arizona Arthritis and Rheumatology Associates, P.C. seeks a Clinical Research Coordinator I to join our team. The CRC coordinates and implements assigned protocols in compliance with FDA CFR, GCP and SOPs, collecting data, assisting in patient assessments, scheduling, and maintaining study files and accountability.

The CRC will recruit participants, manage data entry, and oversee regulatory tasks. Travel to investigator meetings and other sites may be required.

Qualifications

• Must have in-depth knowledge of medical procedures and clinical terminology.
• Possess strong organization and communication skills.
• Ability to develop and maintain strong professional relationships with providers and research subjects.
• Excellent working knowledge of clinical research industry, ICH-GCP Guidelines and all federal regulations.
• Ability to lift 20 pounds.

Responsibilities

• Coordinate observational and clinical research trials assigned.
• Recruit and screen potential participants, review charts, and follow up on referrals.
• Maintain study files, supplies, and medication accountability.
• Keep the clinical trial management system updated with recruited subjects and visits.
• Ensure accurate documentation and reporting of adverse events within timelines.
• Liaise with physicians, staff, and sponsors; participate in monitoring visits.

Skills

Organizational skills

Communication skills

Relationship building

Regulatory knowledge

Clinical research knowledge

Education

Associates Degree or equivalent

Job description

Arizona Arthritis and Rheumatology Associates, P.C. seeks a Clinical Research Coordinator I to join our team. The CRC coordinates and implements assigned protocols in compliance with FDA CFR, GCP and SOPs, collecting data, assisting in patient assessments, scheduling, and maintaining study files and accountability.

The CRC will recruit participants, manage data entry, and oversee regulatory tasks. Travel to investigator meetings and other sites may be required.