Clinical Research Coordinator Jobs in Arizona
Clinical Research Coordinator jobs in Arizona are in strong demand, concentrated in oncology, cardiology, and Phase I through Phase III pharmaceutical trials across a market that ranges from entry-level research assistants to senior coordinators managing multi-site studies. Phoenix, Tucson, and Scottsdale account for the majority of openings, anchored by major employers such as Mayo Clinic, Dignity Health, and Banner Health. Oncology trials and rare disease research are among the most active hiring areas right now. Find a role that fits below and apply directly.
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Showing 5 of 27+ Clinical Research Coordinator jobs
Primary City/State:
Gilbert, ArizonaDepartment Name:
BMDACC Gateway Oncology-RsrchWork Shift:
DayJob Category:
ResearchGood health care is key to a good life. At Banner Health, we understand that, and that’s why we work hard every day to make a difference in people’s lives. We’ve united under a common goal: Make health care easier, so life can be better. It’s a lofty goal, but it’s one we’re committed to seeing through. Do you like the idea of making a positive change in people’s lives – and your own? If so, this could be the perfect opportunity for you. Apply now.
Cancer clinical trials and research are the basis for virtually all advancement in cancer care. Through the careful study and evaluation of new treatments and therapies, clinical trials help uncover better ways to prevent, diagnose and treat cancer. Clinical trials can be a long, careful process. Often, they include many phases and last for many years.
As a Clinical Research Coordinator on our teams, we offer a friendly work environment with career growth opportunities. The department conducts Phases 1-3 treatment clinical trials covering all disease groups with the goal to provide support to the physician investigators and to provide trial treatment options to the patients in a safe and ethical manner, while ensuring compliance to the FDA and institutional regulations. Bring your established Oncology and or Research experience and join a team dedicated to providing an excellent experience to patients.
Schedule: Monday - Friday 8am-4:30pm
Location: 2940 E Banner Gateway Dr BMDACC at Canyon Springs
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 responsible for coordinating and/or implementing assigned protocols. This position includes collecting and recording medical data and history, assisting in patient assessments, and maintaining study files.
CORE FUNCTIONS
1. Provides study information and obtains relevant information to and from patients engaged in clinical studies, which includes: assisting in the recruitment and screening of volunteers; registering patients; providing information on clinical trials and protocols to interested participants in a timely and helpful manner; obtaining relevant medical history on candidates by phone and in person; collecting previous relevant medical records data on patient; explaining procedures and consent forms; compiling all information prior to the initial visit; responding to inquiries from study participants or collateral informants in a timely and helpful manner; updating databases with patient information; and/or, performing other related activities.
2. Performs tasks required by protocol, which may include obtaining patient medical history, systems review, phlebotomy, EKG, and cognitive assessment on patients. Collects vital signs. Maintains quality assurance on designated protocols. Collects data as required and assists in interpreting and evaluating results as required.
3. Triages adverse events and communicates with the research physician regarding the occurrence of adverse events. Collects information regarding indicated medical follow-up with the subject and collateral informants as needed.
4. Provides educational information to patients and their families. Serves as a resource and support person for patients and families by being a consistent person they can contact within the clinical research program. Provides information to the patient and family related to the healthcare of the patient such as health maintenance, prevention, and anticipatory guidance relevant to study-related diseases.
5. Ensures uniform implementation of protocols by completing required documentation in a consistent, accurate and timely manner. Assists in preparing appropriate IRB (Institutional Review Board) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner. May participate in the annual IRB approval and update process.
6. Serves as a liaison to other departments and programmatic areas, as well as community agencies.
7. Ensures that primary referring physicians receive timely progress notes on the patient’s diagnosis and treatment.
8. May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
9. Department level responsibility. Some positions may have frequent interaction with patients, families, visitors, physicians, and related clinical departments.
MINIMUM QUALIFICATIONS
Must possess knowledge of clinical research methodologies as normally obtained by the completion of a bachelors' degree in a healthcare field.
Experience typically gained through two to four years clinical research experience. Familiarity with medical and clinical terminology. Must have excellent organizational and task management skills. Ability to maintain confidentiality of patient and study information. Ability to maintain knowledge of Federal and State regulations governing practice as well as Institute policies and procedures related to medical and nursing practice. Excellent human relations, organizational and communication skills are required.
PREFERRED QUALIFICATIONS
Possession of Clinical Research Coordinator Certification (CRCC).
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:
Gilbert, ArizonaDepartment Name:
BMDACC Gateway Oncology-RsrchWork Shift:
DayJob Category:
ResearchGood health care is key to a good life. At Banner Health, we understand that, and that’s why we work hard every day to make a difference in people’s lives. We’ve united under a common goal: Make health care easier, so life can be better. It’s a lofty goal, but it’s one we’re committed to seeing through. Do you like the idea of making a positive change in people’s lives – and your own? If so, this could be the perfect opportunity for you. Apply now.
Cancer clinical trials and research are the basis for virtually all advancement in cancer care. Through the careful study and evaluation of new treatments and therapies, clinical trials help uncover better ways to prevent, diagnose and treat cancer. Clinical trials can be a long, careful process. Often, they include many phases and last for many years.
As a Clinical Research Coordinator on our teams, we offer a friendly work environment with career growth opportunities. The department conducts Phases 1-3 treatment clinical trials covering all disease groups with the goal to provide support to the physician investigators and to provide trial treatment options to the patients in a safe and ethical manner, while ensuring compliance to the FDA and institutional regulations. Bring your established Oncology and or Research experience and join a team dedicated to providing an excellent experience to patients.
Schedule: Monday - Friday 8am-4:30pm
Location: 2940 E Banner Gateway Dr BMDACC at Canyon Springs
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 responsible for coordinating and/or implementing assigned protocols. This position includes collecting and recording medical data and history, assisting in patient assessments, and maintaining study files.
CORE FUNCTIONS
1. Provides study information and obtains relevant information to and from patients engaged in clinical studies, which includes: assisting in the recruitment and screening of volunteers; registering patients; providing information on clinical trials and protocols to interested participants in a timely and helpful manner; obtaining relevant medical history on candidates by phone and in person; collecting previous relevant medical records data on patient; explaining procedures and consent forms; compiling all information prior to the initial visit; responding to inquiries from study participants or collateral informants in a timely and helpful manner; updating databases with patient information; and/or, performing other related activities.
2. Performs tasks required by protocol, which may include obtaining patient medical history, systems review, phlebotomy, EKG, and cognitive assessment on patients. Collects vital signs. Maintains quality assurance on designated protocols. Collects data as required and assists in interpreting and evaluating results as required.
3. Triages adverse events and communicates with the research physician regarding the occurrence of adverse events. Collects information regarding indicated medical follow-up with the subject and collateral informants as needed.
4. Provides educational information to patients and their families. Serves as a resource and support person for patients and families by being a consistent person they can contact within the clinical research program. Provides information to the patient and family related to the healthcare of the patient such as health maintenance, prevention, and anticipatory guidance relevant to study-related diseases.
5. Ensures uniform implementation of protocols by completing required documentation in a consistent, accurate and timely manner. Assists in preparing appropriate IRB (Institutional Review Board) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner. May participate in the annual IRB approval and update process.
6. Serves as a liaison to other departments and programmatic areas, as well as community agencies.
7. Ensures that primary referring physicians receive timely progress notes on the patient’s diagnosis and treatment.
8. May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
9. Department level responsibility. Some positions may have frequent interaction with patients, families, visitors, physicians, and related clinical departments.
MINIMUM QUALIFICATIONS
Must possess knowledge of clinical research methodologies as normally obtained by the completion of a bachelors' degree in a healthcare field.
Experience typically gained through two to four years clinical research experience. Familiarity with medical and clinical terminology. Must have excellent organizational and task management skills. Ability to maintain confidentiality of patient and study information. Ability to maintain knowledge of Federal and State regulations governing practice as well as Institute policies and procedures related to medical and nursing practice. Excellent human relations, organizational and communication skills are required.
PREFERRED QUALIFICATIONS
Possession of Clinical Research Coordinator Certification (CRCC).
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 27 Clinical Research Coordinator Jobs in Arizona
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Find JobsClinical Research Coordinator Jobs by City in Arizona
Where Arizona roles are concentrated, by current openings.
Clinical Research Coordinator Job Market in Arizona
A snapshot from current Arizona openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
What Arizona Employers Look For
The qualifications that appear most often in clinical research coordinator jobs across Arizona.
- Bachelor's degree in life sciences, nursing, or a related health field required
- ACRP or SOCRA clinical research certification strongly preferred or required
- Minimum one to two years of experience coordinating clinical trials or studies
- Familiarity with FDA regulations, ICH-GCP guidelines, and IRB submission processes
- Proficiency with electronic data capture systems such as REDCap or Medidata Rave
- Strong organizational skills with ability to manage multiple active protocols simultaneously
Clinical Research Coordinator Jobs in Arizona: Frequently Asked Questions
How do you become a clinical research coordinator in Arizona?
Most clinical research coordinator roles in Arizona require a bachelor's degree in a life science, nursing, or public health field. Arizona does not issue a state-specific license for this role, but employers consistently expect national certification through the Association of Clinical Research Professionals or the Society of Clinical Research Associates. Gaining that credential alongside hands-on experience in a clinical or research setting is the standard path Arizona hiring managers look for.
How much do clinical research coordinators make in Arizona?
Clinical research coordinators in Arizona earn a median of about $124,920 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $65,780 for the lowest 10% to over $209,130 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire clinical research coordinators in Arizona?
Employers hiring clinical research coordinators in Arizona right now include University of Arizona, Banner Health, and Arizona Liver Health, based on current listings on Migrate Mate as of August 2026. Arizona's concentration of large integrated health systems and academic medical centers means openings appear consistently rather than seasonally, with oncology and cardiovascular trial programs generating some of the most frequent postings.
Which Arizona cities have the most clinical research coordinator jobs?
Tucson, Phoenix, and Chandler have the most clinical research coordinator openings in Arizona. Phoenix dominates because of its density of major hospital systems and research institutes, while Tucson's presence is driven largely by the University of Arizona Health Sciences and its affiliated trial sites, and Scottsdale attracts openings through its cluster of specialty clinics and private research organizations.
Are there remote clinical research coordinator jobs in Arizona?
Yes, but they're limited, because most coordinator duties involve direct patient contact, site visits, and on-site data collection. About 25% of clinical research coordinator openings tied to Arizona are remote or hybrid as of August 2026, reflecting how hands-on the role typically is. The tasks most commonly done remotely are regulatory document management, data entry, and sponsor correspondence rather than patient-facing coordination work.
How can I get hired as a clinical research coordinator in Arizona with little or no experience?
The most realistic entry point is applying for a clinical research assistant or study coordinator associate role, which large Arizona systems such as Banner Health and Mayo Clinic post as direct stepping stones into full coordinator positions. A background as a medical assistant, phlebotomist, or clinical data specialist transfers well. Completing a Good Clinical Practice certification before applying gives candidates a concrete credential that signals readiness even without trial experience.
Where can I find and apply to clinical research coordinator jobs in Arizona?
You can find and apply to clinical research coordinator jobs in Arizona on Migrate Mate, which lists current Arizona openings from employers actively hiring. Find the roles that fit your experience and specialty area and apply directly through the listings.
See All 27 Clinical Research Coordinator Jobs in Arizona
Find roles in Arizona that match your experience and apply in just a few clicks.
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