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Clinical Trial Transparency Associate Jobs in Arizona

Banner Health

POS15903

Tucson, AZ · On-site

Assistant Professor, Associate Professor, Professor - University of Arizona Cancer Center The ... Experience in writing and developing clinical trial protocols and leading clinical trials is ...

Healix Infusion Therapy

INFUSION NURSE

Sun City, AZ · On-site

$33.50 - $44.50/hr

Bachelor of Science in Nursing (BSN) or Associate Degree in nursing (ADN). * 2+ years' experience ... Clinical trial experience is a plus License and Certifications * State Board of Nursing Licensed ...

Healix Infusion Therapy

INFUSION NURSE

Sun City, AZ · On-site

$35.75 - $47.25/hr

Bachelor of Science in Nursing (BSN) or Associate Degree in nursing (ADN). * 2+ years' experience ... Clinical trial experience is a plus License and Certifications * State Board of Nursing Licensed ...

Healix Infusion Therapy

INFUSION NURSE

Sun City West, AZ · On-site

$35 - $46.50/hr

Bachelor of Science in Nursing (BSN) or Associate Degree in nursing (ADN). * 2+ years' experience ... Clinical trial experience is a plus License and Certifications * State Board of Nursing Licensed ...

Healix Infusion Therapy, LLC

INFUSION NURSE

Sun City, AZ · On-site

$33.50 - $44.50/hr

Bachelor of Science in Nursing (BSN) or Associate Degree in nursing (ADN). * 2+ years' experience ... Clinical trial experience is a plus License and Certifications * State Board of Nursing Licensed ...

Merck & Co.

... trial.Performs clinical study site management/monitoring activities in compliance with ICH-GCP ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

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All JobsClinical Trial Transparency Associate JobsClinical Trial Transparency Associate Jobs in Arizona

Clinical Trial Transparency Associate information

See Arizona salary details

$16

$37

$65

How much do clinical trial transparency associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical trial transparency associate in Arizona is $37.26, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $41.01 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What is a clinical trial transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.

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

The most popular types of Clinical Trial Transparency jobs in Arizona are:

What are popular job titles related to Clinical Trial Transparency Associate jobs in Arizona?

For Clinical Trial Transparency Associate jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Transparency Associate jobs in Arizona look for?

The top searched job categories for Clinical Trial Transparency Associate jobs in Arizona are:

What cities in Arizona are hiring for Clinical Trial Transparency Associate jobs?

Cities in Arizona with the most Clinical Trial Transparency Associate job openings:

Clinical Trial Transparency Associate jobs near you

Clinical Research Specialist

CommonSpirit Health

Phoenix, AZ

Full-time

Re-posted 16 hours ago

CommonSpirit Health rating

7.0

Company rating: 7.0 out of 10

Based on 532 frontline employees who took The Breakroom Quiz

413th of 887 rated healthcare providers

Job description

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.


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 (e.g., GCP, FDA). Your exceptional organizational skills, attention to detail, and ability to communicate effectively will be crucial in this dynamic field.

  • 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.

Required

  • Associates Degree in related field or an equivalent combination of relevant education and job-related experience in lieu of a degree
  • Minimum Two (2) years related experience


Preferred

  • Bachelors Degree in related field
  • Three (3)+ years clinical experience

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