Clinical Research Coordinator: Trials, Recruitment & Data

Arizona Arthritis

Sun City, Northern (AZ, KY)

Hybrid

USD 52,000 - 76,000

Full time

14 days+
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Job summary

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

The CRC will coordinate and implement assigned protocols in compliance with FDA CFR, GCP and SOPs, collecting data, assisting in patient assessments, scheduling, maintaining study files and accountability of study medications. The role requires strong organization, communication, and the ability to build professional relationships with providers and research subjects, with potential

Qualifications

  • Associates Degree or equivalent required.
  • Strong knowledge of medical procedures and clinical terminology.
  • Excellent organization and communication skills.
  • Ability to build professional relationships with providers and subjects.
  • Excellent working knowledge of clinical research industry, ICH-GCP guidelines and federal regs.
  • Ability to lift 20 pounds.

Responsibilities

  • Coordinate observational and clinical research trials assigned.
  • Recruit and screen potential participants and track recruitment goals.
  • Maintain study files, scheduling, and data entry in the study management system.
  • Ensure proper delegation and regulatory compliance, including IRB-related tasks.
  • Assist with informed consent, adverse event reporting, and patient education.
  • Communicate with investigators and staff to ensure protocol compliance.

Skills

Medical terminology
Organization
Communication
Relationship building
ICH-GCP knowledge
Ability to lift 20 pounds

Education

Associates Degree

Job description

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

The CRC will coordinate and implement assigned protocols in compliance with FDA CFR, GCP and SOPs, collecting data, assisting in patient assessments, scheduling, maintaining study files and accountability of study medications. The role requires strong organization, communication, and the ability to build professional relationships with providers and research subjects, with potential

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