Research Quality Compliance (QC) Coordinator

Arizona Liver Health • Tucson, AZ

1d • $60,000 - $75,000 • Onsite

About The Position

Arizona Liver Health (ALH) / Arizona Clinical Trials (ACT) is seeking an experienced Quality Compliance Coordinator (QC) in Tucson, Arizona, with a background in clinical research, quality compliance, and/or regulatory operations. The coordinator helps ensure scientific excellence, patient safety, regulatory compliance, and high-quality clinical data across research activities. This is a full-time, salaried position with a stated annual salary range of $60,000–$75,000, depending on experience. The schedule is Monday through Friday, 8 a.m. to 5 p.m. Some interoffice travel may be required, using a shared company vehicle or mileage reimbursement.

Requirements

• Bachelor’s degree in healthcare, regulatory affairs, biosciences, or a related field.
• Good Clinical Practice (GCP) certification.
• Thorough understanding of regulatory requirements, GCP principles, and biomedical research ethics.
• Experience developing, managing, and reviewing Standard Operating Procedures (SOPs).
• Understanding of and experience developing and supporting Corrective and Preventative Action Plans (CAPA).
• Ability to work independently and in a fast-paced environment, as well as in teams.
• Strong attention to detail, collaboration, verbal and written communication, organization, and task execution skills.
• Computer proficiency with Microsoft Office and understanding of CTMS/EMR software.
• High level of critical thinking.
• Valid documentation and authorization to work in the U.S. for any employer without sponsorship now or in the future.

Nice To Haves

• Master’s degree in healthcare, biosciences, or a related field.

Responsibilities

• Ensure data integrity and patient safety at the research site through quality assurance review and management of clinical research activities.
• Conduct routine data quality assurance checks.
• Review data for deviations, errors, omissions, and inconsistencies.
• Ensure studies are conducted according to applicable site SOPs.
• Work with research staff and the Principal Investigator to address identified issues promptly and appropriately.
• Complete and review CAPAs as needed and review their implementation as needed.
• Work with clinic staff to address audit findings from sponsors, CROs, IRBs, or FDA inspections.
• Ensure required documentation is complete and appropriately filed.
• Liaise with study sponsors to resolve questions or concerns as needed.
• Work with CRCs to ensure understanding of required consistencies between source records and EDC.
• Help train research staff regarding QC as designated.
• Meet with CRAs during monitoring visits to discuss findings and engage other research staff as needed.

Benefits

• Health, dental, and vision coverage, including HSA plans with employer contribution.
• Two weeks of PTO.
• Five days of sick time.
• Seven company holidays and two half-days.
• 401(k) with company match up to 6%.
• Short- and long-term disability.
• Educational assistance.
• Shared company vehicles for required travel.

What This Job Offers

• Job Type: Full-time