Senior Researcher Jobs in Arizona
Senior Researcher jobs in Arizona are concentrated in biomedical sciences, defense and aerospace research, public health, and social policy analysis, with demand strongest at the senior and principal levels. Phoenix, Tucson, and Tempe are the primary hiring hubs, anchored by institutions and employers like Banner Health, Raytheon Technologies, and Arizona State University, all of which maintain active research programs requiring experienced investigators. Bioinformatics, clinical research, and national security analysis are among the most in-demand specializations in the state. Find a role that fits below and apply directly.
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Showing 5 of 10+ Senior Researcher 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 10 Senior Researcher Jobs in Arizona
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Find Senior Researcher JobsSenior Researcher Jobs by City in Arizona
Where Arizona roles are concentrated, by current openings.
Senior Researcher 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 senior researcher jobs across Arizona.
- Advanced degree (master's or PhD) in a relevant discipline recognized by Arizona hiring institutions
- Minimum five years of research experience with demonstrated independent project leadership
- Proficiency in quantitative or qualitative research methods appropriate to the specialization
- Experience securing or managing grants, contracts, or sponsored research funding
- Strong publication record or equivalent technical report and deliverable output
- Familiarity with IRB protocols, data governance standards, or federal compliance requirements
Senior Researcher Jobs in Arizona: Frequently Asked Questions
How do you become a senior researcher in Arizona?
Most senior researcher roles in Arizona require at least a master's degree, and a PhD is expected for positions at universities, state agencies, or major research hospitals. Arizona does not issue a general research license, but clinical researchers working with human subjects must comply with IRB registration requirements, and those in health-related fields may need credentials recognized by the Arizona Medical Board or relevant professional body. Building a record of published or deliverable research is the primary hiring threshold.
Which companies hire senior researchers in Arizona?
Employers hiring senior researchers in Arizona right now include Maverick Power, University of Arizona, and FujiFilm, based on current listings on Migrate Mate as of November 2026. Arizona's concentration of defense contractors, university medical centers, and public health agencies makes it one of the more active states for research hiring outside the coasts.
Which Arizona cities have the most senior researcher jobs?
Phoenix, Tucson, and Arizona account for the largest share of senior researcher openings in Arizona. Phoenix dominates due to its size and the presence of major health systems, defense contractors, and state government research offices, while Tucson benefits from the University of Arizona's research enterprise and nearby federal and military installations, and Tempe draws from Arizona State University's extensive research programs and affiliated industry partners.
Are there remote senior researcher jobs in Arizona?
Yes, and more than many professional fields, since much of senior research work involves data analysis, writing, and collaboration that can be done off-site. About 100% of senior researcher openings tied to Arizona are remote or hybrid as of November 2026, though roles requiring laboratory access, fieldwork, or classified facility clearance remain predominantly on-site. Policy, social science, and data-focused research positions are the most likely to offer full remote arrangements.
How can I get hired as a senior researcher in Arizona with little or no experience?
The most realistic entry path is through a research assistant or associate role at one of Arizona's large research institutions, such as Arizona State University, the University of Arizona, or Banner Health, all of which regularly hire into junior research positions that lead to senior advancement. Completing a graduate program with a research thesis, contributing to funded lab projects, or securing a postdoctoral appointment builds the record employers look for. Certifications in research compliance or IRB coordination give candidates an edge in health and social science settings.
Where can I find and apply to senior researcher jobs in Arizona?
You can find and apply to senior researcher jobs in Arizona on Migrate Mate, which lists current Arizona openings across industries and research disciplines. Search the available roles, find the ones that match your background and specialization, and apply directly to the employers posting them.
See All 10 Senior Researcher Jobs in Arizona
Find roles in Arizona that match your experience and apply in just a few clicks.
Find Senior Researcher Jobs