Job Description
Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood!
Learn more at www.CastleBiosciences.com
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 May 15, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:
Excellent Annual Salary + 20% Bonus Potential
20 Accrued PTO Days Annually + 10 Paid Holidays
401K 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 daily operations of the Clinical Research Department's quality assurance activities, including SOP development, audit preparation, and staff training. The role contributes to the ongoing enhancement of the department's Quality Management System and helps promote a strong quality‑focused culture. Collaboration with Clinical Research, Quality, and Training teams is essential to identify quality issues, assess regulatory and compliance risks, and assist in implementing corrective and preventive actions. The position also plays a key role in internal and external audits by preparing documentation, organizing metrics, and supporting responses to findings. Responsibilities include assisting in the development, implementation, and maintenance of quality assurance plans, protocols, SOPs, and other controlled documents. This position manages document control and learning management systems to ensure accurate version control, record retention, training documentation, and regulatory compliance.
Additional duties include supporting the organization and accessibility of training materials, conducting periodic system audits, and providing technical assistance to document control and LMS users. All activities are carried out in alignment with Castle policies, good clinical practice, and applicable regulatory requirements while upholding professionalism and human subject protection standards.
REQUIREMENTS
Associate degree in related field.
Minimum of 2 years of proven experience in clinical quality assurance, compliance, regulatory, or a related role.
A minimum of 2 years in clinical research.
Actively displays behaviors that support the mission, vision, and values of Castle Biosciences.
PREFERRED QUALIFICATIONS
Bachelor's degree in related field or demonstrated experience as evidence of competency.
Previous experience with complex, global trials.
Current knowledge of U.S., European and/or global regulations and standards covering clinical research.
Basic understanding of ISO 14155 and ISO 13485.
Please see the full job description at the end of the job ad.
SCHEDULE
Monday-Friday, 40 hours per week, exempt position, working from our Phoenix, AZ office location.
READY TO JOIN OUR BIOTECH TEAM?
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!
Castle Biosciences Awards and Research Developments!
WORK AUTHORIZATION
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.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail [email protected].
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please
Learn more at www.CastleBiosciences.com
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 May 15, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:
Excellent Annual Salary + 20% Bonus Potential
20 Accrued PTO Days Annually + 10 Paid Holidays
401K 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 daily operations of the Clinical Research Department's quality assurance activities, including SOP development, audit preparation, and staff training. The role contributes to the ongoing enhancement of the department's Quality Management System and helps promote a strong quality‑focused culture. Collaboration with Clinical Research, Quality, and Training teams is essential to identify quality issues, assess regulatory and compliance risks, and assist in implementing corrective and preventive actions. The position also plays a key role in internal and external audits by preparing documentation, organizing metrics, and supporting responses to findings. Responsibilities include assisting in the development, implementation, and maintenance of quality assurance plans, protocols, SOPs, and other controlled documents. This position manages document control and learning management systems to ensure accurate version control, record retention, training documentation, and regulatory compliance.
Additional duties include supporting the organization and accessibility of training materials, conducting periodic system audits, and providing technical assistance to document control and LMS users. All activities are carried out in alignment with Castle policies, good clinical practice, and applicable regulatory requirements while upholding professionalism and human subject protection standards.
REQUIREMENTS
Associate degree in related field.
Minimum of 2 years of proven experience in clinical quality assurance, compliance, regulatory, or a related role.
A minimum of 2 years in clinical research.
Actively displays behaviors that support the mission, vision, and values of Castle Biosciences.
PREFERRED QUALIFICATIONS
Bachelor's degree in related field or demonstrated experience as evidence of competency.
Previous experience with complex, global trials.
Current knowledge of U.S., European and/or global regulations and standards covering clinical research.
Basic understanding of ISO 14155 and ISO 13485.
Please see the full job description at the end of the job ad.
SCHEDULE
Monday-Friday, 40 hours per week, exempt position, working from our Phoenix, AZ office location.
READY TO JOIN OUR BIOTECH TEAM?
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!
Castle Biosciences Awards and Research Developments!
WORK AUTHORIZATION
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.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail [email protected].
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please
💡 Quick Summary
Seeking a career-building opportunity? The Clinical Research, Internal Quality Assurance Associate position is now open for candidates interested in the Back Office Jobs sector. This role in Phoenix offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Back Office Jobs is a plus.
