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Clinical Data Jobs in Arizona (NOW HIRING)

PHI Health

Clinical Services Coordinator

Tempe, AZ · On-site

This position will assist with data collection and analysis and will function as a clinical resource for Communications Department if needed. This position will report to the Manager Clinical ...

Anovorx Group LLC

Pharmacist - Clinical

Chandler, AZ · On-site

$130K - $136K/yr

This includes gathering and assessing clinical data from patients, creating and supervising care plans, communicating with prescribers to obtain orders, reporting outcomes, making therapeutic ...

PHI Health

Clinical Services Coordinator

Tempe, AZ · On-site

This position will assist with data collection and analysis and will function as a clinical resource for Communications Department if needed. This position will report to the Manager Clinical ...

Banner Health

Senior Data Platform Architect

Phoenix, AZ · On-site +1

$63.75 - $85.25/hr

Banner Health's Data Platform Team is building the modern data platform that runs on Databricks and AWS, supporting everything from claims and clinical data to population health analytics and AI ...

Banner Health

Senior Data Platform Architect

Phoenix, AZ · On-site +1

$63.75 - $85.25/hr

Banner Health's Data Platform Team is building the modern data platform that runs on Databricks and AWS, supporting everything from claims and clinical data to population health analytics and AI ...

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All JobsClinical Data JobsClinical Data Jobs in Arizona

Clinical Data information

See Arizona salary details

$18

$53

$76

How much do clinical data jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical data in Arizona is $53.27, according to ZipRecruiter salary data. Most workers in this role earn between $42.12 and $63.41 per hour, depending on experience, location, and employer.

What is clinical data?

Clinical data refers to information collected during the course of ongoing patient care or as part of a clinical trial program. This data includes patient demographics, medical history, lab results, imaging studies, treatment plans, and outcomes. Clinical data is crucial for informing medical decisions, improving patient care, and supporting medical research and drug development. It is typically collected and managed by healthcare providers, researchers, and data professionals while maintaining strict standards for patient privacy and data security.

What are some common challenges faced by professionals working in clinical data roles, and how can they be addressed?

Professionals in Clinical Data roles often encounter challenges such as managing large volumes of complex data, ensuring data quality and integrity, and adhering to strict regulatory standards. These challenges can be addressed by staying updated on industry best practices, utilizing advanced data management tools, and working closely with cross-functional teams such as clinical research and regulatory affairs. Continuous professional development and effective communication within the team are also key to overcoming these hurdles and ensuring successful clinical trial outcomes.

What are the key skills and qualifications needed to thrive as a clinical data specialist, and why are they important?

To thrive as a Clinical Data Specialist, you need a solid background in life sciences, data management principles, and familiarity with regulatory guidelines, often supported by a relevant degree. Proficiency in clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of standards like CDISC or MedDRA is typically required. Strong attention to detail, analytical thinking, and effective communication skills are crucial soft skills for this role. These competencies ensure the accuracy and integrity of clinical trial data, supporting regulatory compliance and reliable outcomes in clinical research.

What is the difference between Clinical Data vs Clinical Data Coordinator?

AspectClinical DataClinical Data Coordinator
CredentialsTypically requires a degree in health informatics, life sciences, or related fieldRequires similar credentials, often with additional certification in clinical research or data management
Work EnvironmentData analysis, database management, and reporting in healthcare or research settingsOversees data collection, entry, and quality control in clinical trial or healthcare environments
Employer & Industry UsageUsed across hospitals, research institutions, and pharmaceutical companiesCommonly employed in clinical research organizations and hospitals

While both roles involve handling clinical data, Clinical Data professionals focus on data analysis and management, whereas Clinical Data Coordinators oversee data collection and quality assurance in clinical trials or healthcare settings.

What are the most commonly searched types of Clinical Data jobs in Arizona?

The most popular types of Clinical Data jobs in Arizona are:

Clinical Data jobs near you
Infographic showing various Clinical Data job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $110,810 per year, or $53.3 per hour.

Psychiatrist (MD/DO) - Clinical Research

Lighthouse Psychiatry Brain Health Center

Gilbert, AZ • On-site

Contractor

Posted 25 days ago

Job description

Psychiatrist (MD/DO) – Clinical Research

Lighthouse Psychiatry | Arizona
Employment: Part-Time (with potential for Full-Time opportunity)
Focus: Clinical Research | Psychiatry | Clinical Trials

About Lighthouse Psychiatry
Lighthouse Psychiatry is an advanced outpatient mental health practice specializing in evidence-based, interventional psychiatry for patients with complex and treatment-resistant conditions. Our model integrates traditional psychiatric care, psychotherapy, and cutting-edge interventional treatments—including TMS, ketamine-based therapies, and esketamine (Spravato®)—within a highly structured, outcomes-driven clinical environment. Because innovation is our focus, Lighthouse Psychiatry is expanding its clinical research program to advance the development and evaluation of innovative treatments for psychiatric and neurobehavioral conditions.

Position Summary:
Lighthouse Psychiatry is seeking a Board-Certified Psychiatrist (MD/DO) to join our clinical research team to serve as a physician investigator and contributing to industry-sponsored and investigator-initiated clinical research.
This is a research-focused position with responsibilities centered on conducting and overseeing psychiatric clinical trials. Depending on qualifications and experience, the psychiatrist may serve as a Principal Investigator (PI), Sub-Investigator (Sub-I), or physician investigator.
The ideal candidate demonstrates strong clinical judgment, attention to research methodology and protocol adherence, and a commitment to Good Clinical Practice (GCP), research integrity, regulatory compliance, and participant safety.

Clinical Research Responsibilities:
  • Serve as a Principal Investigator (PI), Sub-Investigator, or physician investigator depending on qualifications and study requirements.
  • Provide physician oversight for psychiatric clinical trials.
  • Evaluate prospective research participants and determine medical and psychiatric eligibility.
  • Review and confirm study inclusion and exclusion criteria.
  • Conduct protocol-required psychiatric evaluations and research visits.
  • Participate in and oversee the informed consent process.
  • Perform or oversee protocol-required psychiatric assessments and rating scales.
  • Review medical histories, concomitant medications, laboratory results, ECGs, and other study-related clinical data.
  • Evaluate, document, and follow adverse events (AEs) and serious adverse events (SAEs).
  • Assess the clinical significance and study-treatment relationship of adverse events when required.
  • Ensure appropriate participant safety monitoring throughout study participation.
  • Review and sign source documentation, study records, and investigator documentation as required.
  • Maintain appropriate investigator oversight and ensure adherence to study protocols.
  • Identify, document, and appropriately address protocol deviations.
  • Collaborate with clinical research coordinators and other research personnel.
  • Work with pharmaceutical and biotechnology sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), monitors, central laboratories, pharmacies, and other study vendors.
  • Participate in site qualification, site initiation, monitoring, closeout, and sponsor visits.
  • Attend investigator meetings and study-specific training.
  • Review and respond to clinical and research data queries.
  • Support regulatory documentation and investigator responsibilities.
  • Maintain compliance with ICH-GCP, FDA regulations, IRB requirements, HIPAA, study protocols, and applicable federal and state regulations.
  • Maintain required research training and study-specific certifications.
  • Participate in quality assurance and research compliance activities.
  • Contribute to the development and expansion of Lighthouse Psychiatry's clinical research program.

Principal Investigator Opportunities:
Qualified physicians may have opportunities to assume Principal Investigator responsibilities, including:
  • Overall medical and scientific oversight of assigned clinical trials.
  • Ensuring studies are conducted according to the approved protocol, investigator agreement, GCP, and applicable regulatory requirements.
  • Maintaining appropriate delegation and oversight of research personnel.
  • Reviewing participant eligibility and safety.
  • Reviewing safety reports and clinically significant findings.
  • Ensuring appropriate documentation of protocol deviations and safety events.
  • Providing oversight of investigational product-related clinical decisions.
  • Participating in sponsor and CRO communications.
  • Supporting regulatory inspections and research audits.
  • Reviewing study performance, enrollment, retention, and data quality
  • Maintaining appropriate investigator availability and supervision.

Research & Program Development Opportunities
Depending on experience and interest, opportunities may include:
  • Principal Investigator development and mentorship.
  • Industry-sponsored Phase II–IV psychiatric clinical trials.
  • Investigator-initiated studies.
  • Treatment-resistant depression research.
  • Psychopharmacology research.
  • Neuromodulation research.
  • TMS and brain-stimulation research.
  • Ketamine and emerging therapeutic research.
  • Novel psychiatric medications and investigational therapeutics.
  • Biomarker and neuroscience research.
  • Research protocol development.
  • Scientific presentations, abstracts, posters, and publications.
  • Collaboration with pharmaceutical and biotechnology companies.
  • Collaboration with CROs, academic institutions, and research organizations.
  • Development of new psychiatric clinical trial programs.

Required Qualifications:
  • MD or DO degree from an accredited medical school.
  • Completion of an accredited Psychiatry residency.
  • Board-Certified in Psychiatry.
  • Active, unrestricted Arizona medical license.
  • No state or federal sanctions on medical license.
  • Active DEA registration or eligibility, when required by study responsibilities.
  • Strong psychiatric diagnostic and clinical assessment skills.
  • Ability to evaluate research participants and make independent medical safety decisions.
  • Strong documentation, organizational, and communication skills.
  • Commitment to participant safety, research integrity, and regulatory compliance.

Preferred Qualifications:
  • Previous experience as a Principal Investigator, Sub-Investigator, or clinical research investigator.
  • Experience conducting psychiatric clinical trials.
  • Good Clinical Practice (GCP) certification or willingness to complete required training.
  • Familiarity with FDA-regulated clinical research.
  • Familiarity with IRB processes and human-subject research requirements.
  • Experience with pharmaceutical or biotechnology-sponsored clinical trials.
  • Experience working with CROs and clinical research monitors.
  • Experience with psychiatric rating scales and structured research assessments.
  • Research publications, presentations, or previous academic research experience.
  • Interest in psychopharmacology, neuroscience, treatment-resistant depression, neuromodulation, or emerging psychiatric therapeutics.

Prior clinical research experience is preferred but not required. Psychiatrists with strong clinical experience and an interest in developing expertise as a clinical investigator are encouraged to apply.

What Lighthouse Psychiatry Offers:
  • Dedicated clinical research-focused physician role.
  • Opportunity to participate in innovative psychiatric clinical trials.
  • Clinical research coordinator and administrative research support
  • Opportunities to work with pharmaceutical, biotechnology, and CRO partners.
  • Development pathway toward Principal Investigator (PI) responsibilities.
  • Exposure to emerging psychiatric medications and therapeutic technologies.
  • Opportunities for scientific collaboration and professional development.
  • Potential participation in publications and research presentations.
  • Flexible full-time or part-time structure.
  • Potential research leadership opportunities as the program expands.

Ideal Candidate:
We are seeking a psychiatrist who is interested in advancing psychiatric treatment through clinical research and drug development. The ideal candidate combines strong psychiatric expertise with intellectual curiosity, attention to protocol and data quality, and a commitment to protecting research participants.

Psychiatrists interested in clinical trials, psychopharmacology, neuroscience, treatment-resistant depression, novel therapeutics, and Principal Investigator opportunities are strongly encouraged to apply.

Lighthouse Psychiatry is an Equal Opportunity Employer.

How to Apply:
Qualified candidates should submit a resume/CV and brief cover letter outlining clinical interests and availability. Confirmed active Arizona licensure and compliance with state requirements are required prior to start date.

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