On-Site Clinical Research Coordinator – Tucson

Del Sol Research Management, LLC.; Tucson (AZ); On-site; USD 52,000 - 76,000; Full time

Job summary

Del Sol Research in Tucson, Arizona is seeking a motivated Clinical Research Coordinator to join our trials team. The role focuses on participant management, protocol compliance, sponsor communication, and accurate study documentation.

Candidates with strong clinical experience may start as a Clinical Research Assistant while completing our internal training program before advancing to the coordinator role. This is a full-time, on-site position.

Qualifications

• High School Diploma or GED required.
• Previous clinical experience required.
• Medical Assistant certification or equivalent clinical experience strongly preferred.
• Bachelor's degree in healthcare or science-related field preferred.
• Clinical research experience preferred but not required.
• Strong knowledge of medical terminology and patient care.
• Excellent organization, documentation, communication, and critical-thinking skills.
• Ability to manage multiple studies and deadlines.

Responsibilities

• Coordinate participant study visits across multiple therapeutic areas.
• Recruit, screen, schedule, enroll, and follow research participants.
• Prepare and maintain accurate source documentation and study records.
• Coordinate laboratory, diagnostic, and protocol-required procedures.
• Communicate with sponsors, monitors, investigators, and participants.
• Support monitoring visits, audits, and sponsor meetings.
• Maintain protocol compliance and participant safety.
• Document and report adverse events and protocol deviations as required.

Skills

Medical terminology

Patient care

Organization

Documentation

Communication

Critical thinking

Education

High school diploma or GED

Medical Assistant certification

Bachelor's degree in healthcare or science-related field

Job description

Del Sol Research in Tucson, Arizona is seeking a motivated Clinical Research Coordinator to join our trials team. The role focuses on participant management, protocol compliance, sponsor communication, and accurate study documentation.

Candidates with strong clinical experience may start as a Clinical Research Assistant while completing our internal training program before advancing to the coordinator role. This is a full-time, on-site position.