Clinical Research Coordinator II - Tucson Northwest Office

Position Overview

Arizona Kidney Disease and Hypertension Center (AKDHC) is one of the nation's largest groups of physicians specializing in the care of patients with renal disease. Since 1976, the organization has earned the trust of patients and the respect of the community throughout the Phoenix Metropolitan area and across Arizona.

Clinical Research Coordinator II - AKDHC Tucson Northwest Office
The Clinical Research Coordinator II independently manages the daily operations of assigned clinical trials under the direction of the Clinical Research Operations Manager. This mid-level role is responsible for all aspects of subject participation – from recruitment and informed consent to study visits and data collection. The CRC II ensures protocol compliance, oversees regulatory documentation, serves as the main point of contact for sponsors and monitors, and provides backup and mentorship to junior staff. The role supports both industry-sponsored and investigator-initiated studies across multiple therapeutic areas.

Key Responsibilities

• Independently coordinate all aspects of clinical trials from start-up through close-out.
• Conduct protocol-specific procedures, accurately collect data, and ensure timely electronic data capture.
• Track subject enrollment, study visits, and protocol deviations while proactively resolving issues.
• Maintain audit-ready regulatory binders and support IRB submissions and amendments.
• Mentor and serve as backup for junior staff, including CRC I and Clinical Research Assistants.
• Perform clinical assessments (vital signs, ECGs, specimen collection, and phlebotomy) as needed.
• Identify and report adverse events per protocol and regulatory requirements.
• Participate in departmental meetings, process improvements, and continuing education initiatives.

Required Qualifications

• Excellent patient care skills paired with a positive work ethic.
• Proficiency in clinical trial systems (EDC, IRT, CTMS) and strong technical aptitude.
• Excellent written and verbal communication skills with strong critical thinking and time management.
• Ability to manage multiple trials simultaneously while ensuring protocol compliance.
• Clinical Research Coordinator certification (e.g., ACRP, SOCRA) is required.
• Bachelor's degree in life sciences, nursing, or a related field is preferred.
• 2-5 years of experience coordinating clinical trials in a healthcare or research setting.
• Familiarity with GCP, ICH, and FDA regulatory requirements.

Preferred Qualifications

• Bilingual proficiency is appreciated and considered a valuable asset.

Benefits & Perks

• Competitive Compensation
• Paid time off
• Medical, dental, and vision benefits
• Future growth opportunities and a collaborative, creative environment that supports continuous learning