Clinical Research Quality Compliance Specialist

Arizona Liver Health; Tucson (AZ); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Health, Dental, Vision

2 weeks PTO

5 days Sick Time

Company holidays + 2 half-days

401K with company match

Short & Long Term Disability

Educational Assistance

Shared company vehicles for travel

Job summary

Arizona Liver Health (ALH) in Tucson, AZ, is seeking a Quality Compliance Coordinator (QC) to uphold the highest standards in clinical research conduct. The role emphasizes data integrity, patient safety, and regulatory compliance across the site.

The QC will work with investigators and staff to resolve findings, develop CAPAs, and ensure documentation is complete and properly filed. A Bachelor’s in healthcare or regulatory fields is required, with GCP certification preferred.

Qualifications

• Knowledge of regulatory requirements and GCP in clinical research.
• Experience developing and reviewing SOPs and CAPA programs.
• Ability to work independently in a fast-paced setting and coordinate with teams.

Responsibilities

• Ensure data integrity and patient safety through QA review of study activities.
• Perform routine data quality checks and identify deviations or errors.
• Ensure adherence to site SOPs and address issues with the PI and staff.
• Coordinate CAPA activities and verify implementation with stakeholders.
• Respond to audit findings from sponsors, CROs, IRB or FDA inspections.

Skills

Regulatory requirements

GCP knowledge

Biomedical research ethics

Data quality assurance

Effective communication

Education

Bachelor’s Degree in healthcare/regulatory affairs/biosciences

Master’s Degree preferred

GCP certification

Tools

CTMS/EMR software

SOP development tools

Job description

Arizona Liver Health (ALH) in Tucson, AZ, is seeking a Quality Compliance Coordinator (QC) to uphold the highest standards in clinical research conduct. The role emphasizes data integrity, patient safety, and regulatory compliance across the site.

The QC will work with investigators and staff to resolve findings, develop CAPAs, and ensure documentation is complete and properly filed. A Bachelor’s in healthcare or regulatory fields is required, with GCP certification preferred.