Clinical Research, Internal Quality Assurance Associate

Clinical Research, Internal Quality Assurance Associate Castle Biosciences Inc. is growing, and we are looking to hire a full‑time Clinical Research, Internal Quality Assurance Associate working from our Phoenix, AZ office location, with a start date of September 15, 2026. Why Castle Biosciences? Excellent Annual Salary + 20% Bonus Potential 20 Accrued PTO Days Annually + 10 Paid Holidays 401(k) with 100% Company Match up to 6% 3 Health Care Plan Options + Company HSA Contribution Company Stock Grant Upon Hire A Day in the Life of an Internal Quality Assurance Associate The Internal Quality Assurance Associate supports the day‑to‑day quality assurance operations of the Clinical Research Department by assisting with the implementation and continuous improvement of the Quality Management System (QMS). This role collaborates with Clinical Research, Quality, and Training teams to support quality initiatives, develop and maintain Standard Operating Procedures (SOPs) and controlled documents, manage document control and Learning Management System (LMS) processes, and assist with internal and external audits and regulatory inspections. The associate ensures compliance with CSTL policies, Good Clinical Practice (GCP), and applicable regulatory requirements while promoting quality, supporting staff training, and maintaining the integrity of clinical research activities and human subject protections. Required Qualifications Associate degree in related field. Minimum of 2 years of proven experience in clinical quality assurance, training, compliance, regulatory, or a related role. A minimum of 2 years in clinical research. Fundamental understanding of medical/therapeutic area knowledge and medical terminology. Highly skilled in Microsoft Office, proficiency in Microsoft Word and Excel, and the ability to learn appropriate software. Preferred Qualifications Bachelor's degree in related field or demonstrated experience as evidence of competency. Previous experience with complex, global trials. Competent in study development processes, current industry standards, such as, but not limited to: ICH GCP, ISO 14155, IDE requirements, HIPAA, GDPR guidelines, Quality Management Systems, and 21 CFR Part 11 guidelines. Schedule Monday–Friday, 40 hours per week, exempt position, working from our Phoenix, AZ office location. Application We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile‑friendly application. We're excited to learn more about you and look forward to connecting soon! For more information, or to apply now, you must go to the website below. Please do not email your resume to us as we only accept applications through our website. Equal Opportunity Employer Castle Biosciences is an equal‑opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H‑1B visas, OPT, or employment‑related visas. #J-18808-Ljbffr