Regulatory Affairs Analyst Jobs in Arizona
Regulatory affairs analyst jobs in Arizona are concentrated in pharmaceuticals, medical devices, and biotechnology, with the market anchored by a strong cluster of life sciences employers across the Phoenix metro and Tucson. Companies such as Honeywell, Banner Health, and Microchip Technology have lasting regulatory functions in the state, and demand runs from entry-level coordinators to senior regulatory strategy roles. Submissions management, FDA compliance, and quality systems are the most consistently requested specialties in Arizona postings. See the openings below and apply to the ones that match your experience.
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Showing 5 of 8+ Regulatory Affairs Analyst jobs
Primary City/State:
Phoenix, ArizonaDepartment Name:
HRPP/Regulatory Affairs-RsrchWork Shift:
DayJob Category:
ResearchFind your path in health care. Our team members make Banner Health a Great Place To Work®. Learn how you can join our dedicated team of professionals.
Banner Research is currently seeking a Senior Research Regulatory Affairs Associate to provide regulatory support for facility-based research. All clinical research studies have a myriad of regulatory documents and required submissions. Failure to maintain required documentation and IRB approvals would result in non-compliance with federal regulations. As a facility-based Senior Research Regulatory Affairs Associate, you will provide regulatory support for a variety of types of projects, such as clinical trials, investigator-initiated studies, cooperative studies, chart reviews, and more. Our portfolio includes multiple research areas, such as cardiovascular disease, orthopedics, neurology, pediatrics, pharmacy, and many others. We provide research regulatory support for many of the Banner hospitals and other facilities where research is taking place in multiple states.
As a Senior Research Regulatory Affairs Associate you will work closely with clinicians, coordinators, and other site staff while maintaining an electronic Investigator Site File for all studies. In a typical day, you may assist in making sure documents meet IRB specifications and submit to the IRB, collect and update regulatory documents, and interact with various stakeholders. Every day is different, so an interest in learning about multiple types of studies is a plus. You should be able to stay very organized while multitasking, meeting deadlines, prioritizing your workload, and feel comfortable using online and Microsoft programs. Critical thinking and attention to detail are also important. We spend most of the day on the computer and interacting with staff, clinicians, monitors/sponsors and IRBs.
Schedule: Remote Hybrid: Monday - Friday, 8am-5pm but flexible as long as during regular business hours. .
Banner Alzheimer's Institute (BAI) was established in 2006 as Banner Health's first Center of Excellence. Banner Sun Health Research Institute (BSHRI) was founded in 1986. Our team is uniquely, passionately, and strategically committed to ending Alzheimer's disease and other neurodegenerative disorders without losing another generation, advancing oncology research to improve cancer prevention and treatment outcomes, and providing an unparalleled model of care for families facing these devastating diseases. Banner Research is committed to improving people's lives through comprehensive patient care and advances that capitalize on the best biomedical research. We intend to make a transformational difference in Alzheimer's disease, other neurodegenerative disorders, and oncology research and care.POSITION SUMMARY
This position is expected to demonstrate some degree of personal and professional competency and critical thought processes with guidance. Provides direction for the daily operational coordination for all regulatory aspects of sponsored, grant-funded and/or investigator-initiated research projects. Serves as the professional resource for regulatory information, handles the submission of electronic regulatory documents; maintains electronic site documents. Leads coordination of regulatory activities with sponsors, clinical research organizations (CROs), clinical research staff, institutional review boards (IRBs) and other internal stakeholders.
CORE FUNCTIONS
1. Prepare and submit research applications and perform regulatory study start up activities, edit informed consents and other related documents, may assist Principal Investigators (PIs) with protocol and study-related document development, facilitate completion of ongoing continuation reports to the IRB which include adverse event and protocol deviation reporting, study amendment reporting and complete other submissions to respective IRBs as required.
2.Maintain all electronic regulatory documents including protocols, investigator brochures, consents, and recruiting materials. facilitate completion of continuing reviews and amendments per sponsor, participating institutions, Good Clinical Practice (GCP), FDA and other applicable federal, state and local regulatory agency regulations, policies and procedures, and/or guidelines.
3.Act as site’s regulatory point-person to provide information to the PI, Research Director or Clinical Trial Senior Manager, and study staff regarding IRB submissions and approvals of study-related documents. Maintain protocol status updates for pending and active projects. May participate in departmental meetings, conferences, and educational events.
4.Interact with sponsors and CROs, providing requested regulatory documents throughout the life of a study. Participate in site initiation visits, sponsor monitoring, audits and the FDA inspections for review of electronic regulatory binders. Serve as the liaison and expert regulatory representative and professional resource for assigned projects. Interact with sponsors, participating research institutions, CROs, regulatory agencies, and involved institutional departments on behalf of the PI or the IRB.
5.Coordinate regulatory activities with the needs of research staff or the IRB to ensure timely submission of all regulatory documents and requests of sponsors.
6. Maintain up-to-date knowledge on federal, state, and local research regulatory requirements. Serve as designated regulatory point-person for audits performed by regulatory agencies (i.e., OHRP, ORI, and FDA). Engage in core measures of customer service. Exhibit professional standards to ensure human subjects protection in the conduct of clinical research.
7. Perform other administrative duties as required to support the senior regulatory staff or the site’s RD or CTSM.
MINIMUM QUALIFICATIONS
Requires a bachelor’s degree in business, healthcare administration or science related field or at least two to three years of substantial and ongoing professional experience working in the research regulatory environment. In addition, an equivalent combination of education and experience may be allowed.
Must have professional designations such as Certified Clinical Research Professional (CCRP®), or Certified Clinical Research Coordinator (CCRC®) or equivalent additional years of direct research regulatory experience.
Must possess knowledge and understanding of the applicable regulatory requirements, as well as the commonly accepted concepts, practices and procedures within the research regulatory arena. In addition, must be able to use them in varied situations. Ability to plan, organize, set priorities, and work in a fast paced environment and handle multiple projects. Demonstrated capacity to problem solve, think critically and creatively, and provide assistance through a consultative role. Interpersonal skills necessary to establish and maintain effective working relationships.
Computer proficiency including, but not limited to: operational knowledge of Microsoft Office computer applications (such as MS Word, Outlook, Excel), ability to locate and synthesize information on the internet, experience working with CTMS (Complion, iRIS).
PREFERRED QUALIFICATIONS
Additional related education and/or experience preferred.
EEO Statement:
EEO/Disabled/Veterans
Our organization supports a drug-free work environment.
Privacy Policy:
Privacy Policy
Primary City/State:
Phoenix, ArizonaDepartment Name:
HRPP/Regulatory Affairs-RsrchWork Shift:
DayJob Category:
ResearchFind your path in health care. Our team members make Banner Health a Great Place To Work®. Learn how you can join our dedicated team of professionals.
Banner Research is currently seeking a Senior Research Regulatory Affairs Associate to provide regulatory support for facility-based research. All clinical research studies have a myriad of regulatory documents and required submissions. Failure to maintain required documentation and IRB approvals would result in non-compliance with federal regulations. As a facility-based Senior Research Regulatory Affairs Associate, you will provide regulatory support for a variety of types of projects, such as clinical trials, investigator-initiated studies, cooperative studies, chart reviews, and more. Our portfolio includes multiple research areas, such as cardiovascular disease, orthopedics, neurology, pediatrics, pharmacy, and many others. We provide research regulatory support for many of the Banner hospitals and other facilities where research is taking place in multiple states.
As a Senior Research Regulatory Affairs Associate you will work closely with clinicians, coordinators, and other site staff while maintaining an electronic Investigator Site File for all studies. In a typical day, you may assist in making sure documents meet IRB specifications and submit to the IRB, collect and update regulatory documents, and interact with various stakeholders. Every day is different, so an interest in learning about multiple types of studies is a plus. You should be able to stay very organized while multitasking, meeting deadlines, prioritizing your workload, and feel comfortable using online and Microsoft programs. Critical thinking and attention to detail are also important. We spend most of the day on the computer and interacting with staff, clinicians, monitors/sponsors and IRBs.
Schedule: Remote Hybrid: Monday - Friday, 8am-5pm but flexible as long as during regular business hours. .
Banner Alzheimer's Institute (BAI) was established in 2006 as Banner Health's first Center of Excellence. Banner Sun Health Research Institute (BSHRI) was founded in 1986. Our team is uniquely, passionately, and strategically committed to ending Alzheimer's disease and other neurodegenerative disorders without losing another generation, advancing oncology research to improve cancer prevention and treatment outcomes, and providing an unparalleled model of care for families facing these devastating diseases. Banner Research is committed to improving people's lives through comprehensive patient care and advances that capitalize on the best biomedical research. We intend to make a transformational difference in Alzheimer's disease, other neurodegenerative disorders, and oncology research and care.POSITION SUMMARY
This position is expected to demonstrate some degree of personal and professional competency and critical thought processes with guidance. Provides direction for the daily operational coordination for all regulatory aspects of sponsored, grant-funded and/or investigator-initiated research projects. Serves as the professional resource for regulatory information, handles the submission of electronic regulatory documents; maintains electronic site documents. Leads coordination of regulatory activities with sponsors, clinical research organizations (CROs), clinical research staff, institutional review boards (IRBs) and other internal stakeholders.
CORE FUNCTIONS
1. Prepare and submit research applications and perform regulatory study start up activities, edit informed consents and other related documents, may assist Principal Investigators (PIs) with protocol and study-related document development, facilitate completion of ongoing continuation reports to the IRB which include adverse event and protocol deviation reporting, study amendment reporting and complete other submissions to respective IRBs as required.
2.Maintain all electronic regulatory documents including protocols, investigator brochures, consents, and recruiting materials. facilitate completion of continuing reviews and amendments per sponsor, participating institutions, Good Clinical Practice (GCP), FDA and other applicable federal, state and local regulatory agency regulations, policies and procedures, and/or guidelines.
3.Act as site’s regulatory point-person to provide information to the PI, Research Director or Clinical Trial Senior Manager, and study staff regarding IRB submissions and approvals of study-related documents. Maintain protocol status updates for pending and active projects. May participate in departmental meetings, conferences, and educational events.
4.Interact with sponsors and CROs, providing requested regulatory documents throughout the life of a study. Participate in site initiation visits, sponsor monitoring, audits and the FDA inspections for review of electronic regulatory binders. Serve as the liaison and expert regulatory representative and professional resource for assigned projects. Interact with sponsors, participating research institutions, CROs, regulatory agencies, and involved institutional departments on behalf of the PI or the IRB.
5.Coordinate regulatory activities with the needs of research staff or the IRB to ensure timely submission of all regulatory documents and requests of sponsors.
6. Maintain up-to-date knowledge on federal, state, and local research regulatory requirements. Serve as designated regulatory point-person for audits performed by regulatory agencies (i.e., OHRP, ORI, and FDA). Engage in core measures of customer service. Exhibit professional standards to ensure human subjects protection in the conduct of clinical research.
7. Perform other administrative duties as required to support the senior regulatory staff or the site’s RD or CTSM.
MINIMUM QUALIFICATIONS
Requires a bachelor’s degree in business, healthcare administration or science related field or at least two to three years of substantial and ongoing professional experience working in the research regulatory environment. In addition, an equivalent combination of education and experience may be allowed.
Must have professional designations such as Certified Clinical Research Professional (CCRP®), or Certified Clinical Research Coordinator (CCRC®) or equivalent additional years of direct research regulatory experience.
Must possess knowledge and understanding of the applicable regulatory requirements, as well as the commonly accepted concepts, practices and procedures within the research regulatory arena. In addition, must be able to use them in varied situations. Ability to plan, organize, set priorities, and work in a fast paced environment and handle multiple projects. Demonstrated capacity to problem solve, think critically and creatively, and provide assistance through a consultative role. Interpersonal skills necessary to establish and maintain effective working relationships.
Computer proficiency including, but not limited to: operational knowledge of Microsoft Office computer applications (such as MS Word, Outlook, Excel), ability to locate and synthesize information on the internet, experience working with CTMS (Complion, iRIS).
PREFERRED QUALIFICATIONS
Additional related education and/or experience preferred.
EEO Statement:
EEO/Disabled/Veterans
Our organization supports a drug-free work environment.
Privacy Policy:
Privacy Policy
See All 8 Regulatory Affairs Analyst Jobs in Arizona
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Find JobsRegulatory Affairs Analyst Jobs by City in Arizona
Where Arizona roles are concentrated, by current openings.
Regulatory Affairs Analyst Job Market in Arizona
A snapshot from current Arizona openings, updated as new roles post.
Who's Hiring
What Arizona Employers Look For
The qualifications that appear most often in regulatory affairs analyst jobs across Arizona.
- Bachelor's degree in life sciences, engineering, chemistry, or a related technical field
- Working knowledge of FDA regulations including 21 CFR Parts 11, 820, or 211
- Experience preparing and submitting regulatory documents such as 510(k)s or NDAs
- Familiarity with quality management systems and ISO 13485 or ICH guidelines
- Strong technical writing skills for regulatory submissions and SOPs
- Proficiency with document management systems and regulatory information databases
Regulatory Affairs Analyst Jobs in Arizona: Frequently Asked Questions
How do you become a regulatory affairs analyst in Arizona?
Most regulatory affairs analyst positions in Arizona require a bachelor's degree in a life sciences, engineering, or health-related field, and employers in the Phoenix and Tucson markets strongly favor candidates with hands-on experience in FDA-regulated industries. Arizona does not issue a state-specific license for this role, but earning the Regulatory Affairs Certification through the Regulatory Affairs Professionals Society signals credibility and is increasingly preferred by Arizona's medical device and pharmaceutical employers.
Which companies hire regulatory affairs analysts in Arizona?
Companies currently hiring regulatory affairs analysts in Arizona include INNOVATIVE HEALTH, Katalyst Healthcares & Life Sciences, and Stryker, per current listings on Migrate Mate as of November 2026. Arizona's concentration of medical device manufacturers and pharmaceutical operations in the Greater Phoenix corridor means these employers regularly maintain active regulatory teams.
Which Arizona cities have the most regulatory affairs analyst jobs?
The cities with the most regulatory affairs analyst openings in Arizona are Scottsdale, Phoenix, and Tempe. The Phoenix metro drives the majority of postings due to its dense cluster of medical device manufacturers, pharmaceutical operations, and large healthcare systems, while Tucson contributes a meaningful share tied to its life sciences research institutions and defense-adjacent technology companies.
Are there remote regulatory affairs analyst jobs in Arizona?
Yes, and more than most fields, because regulatory affairs work is largely document-driven and does not require a physical presence on a production floor. About 100% of regulatory affairs analyst openings tied to Arizona are remote or hybrid as of November 2026, reflecting how well the role translates to distributed work. Submissions management, regulatory writing, and literature review functions tend to be the most frequently offered in remote or hybrid formats.
How can I get hired as a regulatory affairs analyst in Arizona with little or no experience?
The most realistic entry path is moving laterally from a quality assurance, clinical operations, or laboratory role inside an FDA-regulated company, since Arizona's medical device and pharmaceutical employers, including those operating manufacturing sites in the East Valley and Tucson, regularly hire regulatory coordinators from their own quality teams. Pursuing the Regulatory Affairs Certification as a candidate, completing an internship through Arizona State University's biomedical programs, or targeting associate regulatory affairs roles at contract research organizations based in Phoenix are all concrete steps that give first-time applicants a competitive edge.
Where can I find and apply to regulatory affairs analyst jobs in Arizona?
You can find and apply to regulatory affairs analyst jobs in Arizona on Migrate Mate, which lists current Arizona openings from employers across the state. Search the available roles, find the ones that fit your background and location preferences, and apply directly to the positions that match your experience.
See All 8 Regulatory Affairs Analyst Jobs in Arizona
Find roles in Arizona that match your experience and apply in just a few clicks.
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