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  3. Clinical Research Associate
St. Joseph Hospital & Medical Center logo

Clinical Research Associate

St. Joseph Hospital & Medical Center·Phoenix, Arizona

$36 - $53/hrOtherOn Site2-5 yrsPosted 27 days ago
Practice for this role

Clinical Research Associate · $36 - $53/hr

How this role compares

Computed from live listings

  • -2% vs. median posted rate for allied health roles in Phoenix, Arizona ($36.50/hr, n=175)
  • 364 similar openings in the Phoenix area · median $35.45/hr
$3.00/hr · lowesthighest · $91.52/hr
this role: $35.62/hrmedian $36.50/hr

Shaded band: the middle 50% of 175 posted allied health roles in Phoenix, Arizona rates. This role sits in the 46th percentile.

About the role

Pay for this role is about 2% below the Phoenix, Arizona median for allied health roles.

The Clinical Research Associate will manage and execute clinical trials, ensuring data integrity, patient safety, and regulatory compliance. Responsibilities include conducting site monitoring visits, managing trial documentation, and acting as a liaison between the research organization and study sites.

Where You’ll Work Hello Humankindness

  • Join a Legacy of Healing at Saint Joseph’s Hospital and Medical Center (SJHMC) Ready to make a real difference? Join SJHMC in Phoenix AZ., a 571-bed nonprofit founded by the Sisters of Mercy over 125 years ago. We're more than a hospital; we're a global destination for life-changing care, embracing patients with humankindness. Here, your calling will flourish. We're not just a workplace; we're a community dedicated to a mission of service.
  • Leaders in
  • Specialized
  • Care:
  • Barrow
  • Neurological
  • Institute (BNI): A world-renowned center for groundbreaking neurological research and innovative treatments.
  • Norton
  • Thoracic
  • Institute (NTI): A national leader in advanced thoracic care with pioneering surgical techniques.
  • Level
  • I
  • Trauma
  • Center: One of Arizona's busiest ERs, providing immediate, comprehensive care for critically injured patients 24/7. Why SJHMC?
  • Culture of
  • Excellence &
  • Well-being: We care for our people, fostering professional and personal growth.
  • Community &
  • Collaboration: Be part of a network committed to global health and well-being.
  • Join a
  • Legacy,
  • Shape a
  • Future: Over 20% of our patients travel internationally for our specialized care. This is an invitation to join a family of dedicated professionals at the forefront of medical innovation, united by the power of humankindness. Job Summary and Responsibilities As our Clinical Research Professional you will be instrumental in advancing medical knowledge by expertly managing and executing clinical trials. You will ensure the highest standards of data integrity patient safety and regulatory compliance throughout the research process. Every day you will manage trial activities including participant recruitment data collection and documentation serving as a key liaison for all stakeholders. You will ensure strict adherence to protocols and regulatory requirements from study initiation to completion. To be successful in this role you will bring relevant clinical research experience and a strong understanding of regulatory guidelines. Your exceptional organizational skills attention to detail and ability to communicate effectively will be crucial in this dynamic field. At Barrow Neurological Institute (BNI) one of the world’s premier neuroscience centers we are leading groundbreaking multicenter clinical research to accelerate discoveries for people living with amyotrophic lateral sclerosis (ALS). As part of our Academic Clinical Research Organization (CRO) you will join a nationally recognized team coordinating NIH/NINDS funded studies that are changing how ALS is diagnosed monitored and ultimately treated. We are seeking a motivated Clinical Research Associate (CRA) to support field monitoring activities across a network of leading academic medical centers participating in innovative ALS clinical research studies. This role offers the opportunity to work alongside dedicated research sites while ensuring the highest standards of participant safety regulatory compliance and data quality.

Requirements

Candidates must have a bachelor's degree in a clinical, science, or health-related field or five years of equivalent work experience. A minimum of two years of clinical research experience and proficiency with Microsoft Office Suite are required.

  • bachelor degree
  • Reporting
  • Mentorship
  • Project management
  • Quality control
  • Regulatory compliance
  • Data integrity
  • Protocol adherence
  • FDA regulations
  • Clinical monitoring
  • Site management
  • HIPAA guidelines
  • Participant recruitment
  • ICH/GCP guidelines
  • Clinical trial administration
  • Site feasibility assessment

Posting details

Employment type
Other
Work arrangement
On Site
Experience
2-5 yrs
Salary
$36 - $53/hr
Location
Phoenix, Arizona
Posted
Aug 21, 2026
Closes
Aug 21, 2027
Application
Employer website
St. Joseph Hospital & Medical Center logo

Hiring organization

St. Joseph Hospital & Medical Center

Located conveniently in the heart of Phoenix, Arizona, St. Joseph’s Hospital and Medical Center is a 450+ bed, not-for-profit hospital that provides a wide range of health, social and support services. We are extremely proud to be a nationally recognized center for quality...

IndustryHospitals and Health Care
TypeNonprofit
Size5,001-10,000 employees
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  • Position responsibilities include: Responsible for all aspects of clinical monitoring site management and trial administration as prescribed in the monitoring plan and as instructed by program leadership. Employee is responsible for working with sites during study start up including assessing site feasibility as required provide ongoing training and site initiation visits conducting remote monitoring and approx. 25-30 interim onsite and closeout field monitoring visits located throughout the US and Canada. During each monitoring visit the CRA is responsible for the evaluation of clinical data documentation regulatory document review monitor safety and conduct of study to ensure investigator and site compliance with study protocol overall clinical objectives FDA regulations ICH/GCP guidelines institutional/ CRO SOPs and HIPAA guidelines. The CRA is expected to work cooperatively with study team and operations management to proactively drive project success. Completes preparation and submission of accurate and timely monitoring reports and other requested deliverables as outlined in the Study Monitoring Plan or as requested by program leadership. Effective long-term planning/scheduling of remote and on-site monitoring visits in accordance with the Study Monitoring Plan or as requested by program leadership. Perform Lead Study Monitoring activities as assigned including acting as the primary liaison between BNI CRO and the Clinical Study Sponsor to ensure BNI CRO provides quality monitoring and site management customer services. The Lead Study Monitor will be responsible for the timely review of all monitoring deliverables conduct co-monitoring visits and mentorship of CRA team members. Participates in the quality control process for assigned monitoring activities and makes contributions to improve and adapt quality control procedures including the development of internal corrective and preventative action plans if needed and align service goals with internal and external client expectations Proactively participate in program development. This includes making contributions to the overall quality improvement of clinical monitoring services as well as actively collaborating with program leadership to expand and grow the CRO's professional portfolio. Job Requirements Required Bachelors degree or its international equivalent in clinical, science, or health related field from an accredited institution or five (5) years equivalent work experience in lieu of the degree Two (2)+ years of clinical research experience Experience with
  • Microsoft
  • Office
  • Suite
  • Systems
  • Preferred
  • Registered
  • Nurse:
  • AZ
  • Physical
  • Therapist:
  • AZ
  • Occupational
  • Therapist: AZ and Clinical Research Associate Certified Clinical Research Professional
  • Market context

    Arizona Clinical Research Associate Market

    Clinical Research Associate roles in Arizona typically favor candidates with clinical research monitoring experience, strong Good Clinical Practice (GCP) knowledge, and the ability to manage site documentation and coordinate with study teams. Competition can be stronger for applicants who demonstrate consistent site oversight and organized communication. The requirements and benefits here are AI-summarized from the original job description, saving research time; review the source details and tailor your application to monitoring responsibilities.

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