Clinical Research Specialist

SupportFinity™

Goodyear, AZFull-timePosted Apr 12, 2026

24.33–36.19 an hour

Behavioral Health Market Context

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Job Description

on, 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 (e.g., GCP, FDA). Your exceptional organizational skills, attention to detail, and ability to communicate effectively will be crucial in this dynamic field.
Responsibilities
• Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability.
• Provides study specific, individualized education to study subjects and families.
• Ensures all appropriate subject consents are obtained.
• Collects and processes protocol required specimens.
• Acts as a liaison between Sponsor, Investigator, and Study Subject
• Collects all required study data and completes CRFs in a timely, accurate manner.
Qualifications

Required
• Associates degree or equivalent in a related field or an equivalent combination of relevant education and job-related experience in lieu of a degree, upon hire
• Minimum 2 years related research experience

Preferred
• Bachelors degree or equivalent in a related field and 3+ years clinical experience
Where you'll work

Hello human kindness Located conveniently in the heart of Phoenix, Arizona, St. Joseph's Hospital and Medical Center is a 571-bed, not-for-profit hospital that provides a wide range of health, social and support services. Founded in 1895 by the Sisters of Mercy, St. Joseph's was the first hospital in the Phoenix area. More than 125 years later, St. Joseph's remains dedicated to its mission of caring for the poor and underserved.

We are extremely proud to be a nationally recognized center for quality qua ternary care, medical education and research. St. Joseph's includes the internationally renowned Barrow Neurological Institute, Norton Thoracic Institute, Cancer Center eph's, Ivy Brain Tumor Center, and St. Joseph's Level I Trauma Center (which is verified by the American College of Surgeons). The hospital is also a respected center for high-risk obstetrics, neuro-rehabilitation, orthopedics, and other medical services.

St. Joseph’s is considered a sought-after destination hospital for treating the most complex cases from throughout the world. Every day, approximately 20 percent of the hospital’s patients have traveled from outside of Arizona and the United States to seek treatment eph’s. U.S News & World Report routinely ranks St. Joseph's among the top hospitals in the United States for neurology and neurosurgery.

In addition, St. Joseph's boasts the Creighton University School of Medicine eph's, and a strategic alliance with Phoenix Children's Hospital. St. Joseph's is consistently named an outstanding place to work and one of Arizona's healthiest employers. Come grow your career with one of Arizona's Most Admired Companies.
Pay

$24.33 - $36.19 /hour
Job details

Job code: EX-D6

FACCE8

Job type:
Full-time

Location:

Arizona

About the company:

Common Spirit Health
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Qualifications

  • To be successful in this role, you will bring relevant clinical research experience and a strong understanding of regulatory guidelines (e.g., GCP, FDA)
  • Your exceptional organizational skills, attention to detail, and ability to communicate effectively will be crucial in this dynamic field
  • Associates degree or equivalent in a related field or an equivalent combination of relevant education and job-related experience in lieu of a degree, upon hire
  • Minimum 2 years related research experience

Benefits

  • $24.33 - $36.19 /hour

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
  • Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability
  • Provides study specific, individualized education to study subjects and families
  • Ensures all appropriate subject consents are obtained
  • Collects and processes protocol required specimens
  • Acts as a liaison between Sponsor, Investigator, and Study Subject
  • Collects all required study data and completes CRFs in a timely, accurate manner


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