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Clinical Trial Risk Based Monitoring Jobs in Arizona

YO AI Labs

Oncology Expert - Remote

Phoenix, AZ · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

YO AI Labs

Hematology Expert - Remote

Phoenix, AZ · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

IQVIA

Senior Global Clinical Study Manager

Gilbert, AZ · On-site

... trial site management activities across global studies. This role ensures successful site selection ... Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize ...

IQVIA

Senior Global Clinical Study Manager

Gilbert, AZ

... trial site management activities across global studies. This role ensures successful site selection ... Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize ...

IQVIA

Senior Global Clinical Study Manager

Phoenix, AZ · On-site

... trial site management activities across global studies. This role ensures successful site selection ... Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize ...

IQVIA

Senior Global Clinical Study Manager

Phoenix, AZ

... trial site management activities across global studies. This role ensures successful site selection ... Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize ...

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Clinical Trial Risk Based Monitoring information

What is clinical trial risk based monitoring?

Clinical Trial Risk Based Monitoring (RBM) is a strategy used in clinical research to prioritize and focus monitoring activities on the most critical risks to patient safety and data integrity. Instead of monitoring every data point equally, RBM uses data analytics and risk assessment tools to identify which sites, processes, or data require more attention. This approach increases efficiency, reduces costs, and helps ensure that potential issues are detected and addressed promptly. RBM is supported by regulatory agencies and is increasingly adopted in both large and small clinical trials.

How does a clinical trial risk based monitoring professional typically collaborate with cross-functional teams during a study?

In a Clinical Trial Risk Based Monitoring role, you will regularly work with clinical research associates, data managers, statisticians, and regulatory teams to identify and address potential risks throughout a study. Collaboration often involves participating in meetings to review data trends, sharing insights about site performance, and helping to develop mitigation strategies. Effective communication is crucial, as you will be responsible for ensuring that all stakeholders are informed of key risks and recommended actions. This collaborative environment helps drive patient safety, data integrity, and overall trial success.

What are the key skills and qualifications needed to thrive in clinical trial risk based monitoring, and why are they important?

To thrive in Clinical Trial Risk Based Monitoring, you need expertise in clinical research, regulatory compliance, and data analysis, usually supported by a degree in life sciences or related fields. Familiarity with risk assessment tools, EDC (Electronic Data Capture) systems, and GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, critical thinking, and effective communication help professionals proactively identify and address potential risks in trials. These skills are crucial for maintaining data integrity, ensuring patient safety, and optimizing the efficiency and quality of clinical studies.

What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?

AspectClinical Trial Risk Based MonitoringClinical Trial Data Manager
Primary FocusMonitoring trial sites for risks and complianceManaging and ensuring accuracy of trial data
Required SkillsMonitoring protocols, regulatory knowledge, site managementData management, database systems, quality control
Work EnvironmentClinical sites, monitoring visits, remote oversightData centers, clinical trial databases, office setting
CertificationsGCP, monitoring certificationsCDMP, data management certifications

While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.

What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Arizona?

For Clinical Trial Risk Based Monitoring jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Arizona look for?

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Arizona are:

What cities in Arizona are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities in Arizona with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Risk Based Monitoring jobs near you
Infographic showing various Clinical Trial Risk Based Monitoring job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 13% Part Time, 2% Temporary, and 6% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Clinical Research Coordinator - Phoenix, Arizona

Phoenix, AZ • On-site

MissionHires
See more jobs at MissionHiresexternal

$24 - $32/hr

Other

Posted 8 days ago

Job description

Macoa Health is seeking a Clinical Research Coordinator who is fluent in Spanish and eager to grow within a dynamic, patient-focused clinical trial environment. The ideal candidate will manage daily clinical trial operations, ensure regulatory compliance, and serve as a primary point of contact for patients and sponsors.

Responsibilities
  • Coordinate all aspects of clinical trial conduct from pre-study through close-out.
  • Recruit and consent patients according to study protocols.
  • Ensure accurate data entry and query resolution within study timelines.
  • Maintain essential documents and assist with IRB submissions.
  • Communicate effectively with sponsors, monitors, and study teams.
Requirements
  • Bachelor’s degree in health sciences or related field preferred.
  • Minimum 1 year of clinical research experience.
  • Strong organizational and communication skills.
  • Bilingual in Spanish and English (required).
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