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Clinical Trial Transparency Associate Jobs in Arizona

Relevant experience in clinical trial programming, clinical data analysis, statistical programming ... Pay Transparency * A reasonable estimate of the annual base salary for this position is $90,000 ...

In compliance with pay transparency laws, pay ranges are provided for positions in locations where required. Please note, the final agreed upon compensation is based on individual education ...

In compliance with pay transparency laws, pay ranges are provided for positions in locations where required. Please note, the final agreed upon compensation is based on individual education ...

... clinical trial agreements, technology and data use agreements, and high-value service contracts ... Knowledge of audit, transparency, and records retention requirements applicable to public research ...

... Level Associates Degree Travel Percentage None Category Other Positions Description Us Heart and ... Management of Clinical Trials/Clinical Trial Coordination. * Scheduling follow-up appointments for ...

... clinical trial agreements, technology and data use agreements, and high-value service contracts ... Knowledge of audit, transparency, and records retention requirements applicable to public research ...

POS15902

Tucson, AZ · On-site

$189/hr

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

Showing results 21-40

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

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

Clinical Research Specialist

St Joseph Hospital & Medical Center

Phoenix, AZ • On-site

$24.33 - $36.19/hr

Full-time

Re-posted 29 days ago


Job description


Job Summary and Responsibilities

As our Clinical Research Specialist 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.

The Lonnie and Muhammad Ali Movement Disorder Center is searching for an experienced clinical research coordinator to fill our Clinical Research Specialist position.  The position is responsible for the conduct of clinical research studies under the oversight of the principal investigator.  Responsibilities will include recruiting, maintaining study logs, conducting informed consent discussions, scheduling and completing study visits per protocol and completing required visit documentation.  The Clinical Research Specialist will be the primary liaison with study sponsors through the conduct of the study.  Previous experience with Parkinson’s disease studies is preferred.  The ability to multi-task and remain organized in a high volume clinical trial setting is required. Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. 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. Ensures study documents are maintained in compliance with applicable regulations, guidelines, and policies (i.e. FDA, OHRP, IRB). Collaborates with Investigator to identify adverse events/ serious adverse events to ensure study subject safety and accurate and timely reporting. Ensures appropriate internal and external customer service by demonstrating professional interactions with Sponsor, study monitors, and other departments. Complies with all regulatory and policy requirements. Demonstrates knowledge of federal and state regulations, guidelines, and policies governing the conduct of clinical trials.

The Parkinson’s and Movement Disorders Division is seeking a Clinical Research Specialist to join our team. As as a Parkinson’s Foundation Center of Excellence, and Huntington’s disease Center of Excellence, we strive to offer the best care to our patients. We are also a world leader in Deep Brain Stimulation (DBS) surgery for the treatment of movement disorders.

Our research division continues to expand offering cutting edge research and excellent patient care!

Job Requirements

Required

  • Associates degree in related field or an equivalent combination of relevant education and/ or job-related experience in lieu of degree 
  • Minimum of Two (2) years related experience 
  • Competent in computer skills including the Microsoft Office products

Preferred

  • Three (3) years clinical research experience
  • Bachelor's Degree in related field 
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.

Qualifications:

Required

  • Associates degree in related field or an equivalent combination of relevant education and/ or job-related experience in lieu of degree 
  • Minimum of Two (2) years related experience 
  • Competent in computer skills including the Microsoft Office products

Preferred

  • Three (3) years clinical research experience
  • Bachelor's Degree in related field 
Employment Type: Full Time