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Clinical Trial Risk Based Monitoring Jobs in Arizona

Actalent

Clinical Research Coordinator

Phoenix, AZ · On-site

$58K - $68K/yr

... based on study protocols and inclusion/exclusion criteria. * Support clinical research activities for multiple therapeutic areas, including oncology studies. * Coordinate day-to-day clinical trial ...

ECN Operating LLC

Physician - Psychiatrist

Chandler, AZ · On-site

$120 - $180/hr

Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols ... Provide medical oversight for clinical trial participants, including safety assessments, adverse ...

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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 Dermatology - Tucson, AZ

ProTouch Staffing

Tucson, AZ

Other

Posted 12 days ago

Job description

Job Title: Clinical Research DermatologistLocation: Tucson, AZSchedule: Part-Time (0-8 hours/week)
Start Date: ASAP
About the Role:

We are seeking a board-certified Dermatologist to join as a Clinical Research Dermatologist. In this role, you will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to support Phase I-IV clinical trials.

Key Responsibilities:
  • Serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology and multi-therapeutic clinical trials
  • Conduct medical screenings, dermatological assessments, and physical examinations for study participants
  • Provide clinical oversight and ensure patient safety in accordance with study protocols, ICH-GCP, and regulatory guidelines
  • Collaborate with study coordinators, nurses, and research staff to maintain compliance and accurate documentation
  • Document patient interactions, adverse events (AEs/SAEs), and maintain records in EHR/EDC systems
  • Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs
  • Participate in site initiation visits (SIVs), monitoring visits, and audits
  • Contribute to protocol feasibility, study design input, and patient recruitment strategies
  • Attend investigator meetings and provide clinical expertise on dermatology endpoints and safety monitoring
  • Stay up to date with clinical research regulations and advancements in dermatology
Qualifications:
  • M.D. or D.O. with an active, unrestricted Arizona medical license
  • Board-certified in Dermatology
  • Valid DEA license and BLS/ACLS certification
  • Prior clinical research/trial experience preferred (training available for suitable candidates)
  • Proficiency in EHR systems and clinical trial platforms (EDC, CTMS)
  • Strong communication and interpersonal skills
  • Ability to work in a fast-paced, multidisciplinary environment
  • Commitment to ethical research practices and patient-centered care
Compensation & Benefits:
  • Competitive hourly rate: Open to negotiate (based on experience)
  • Flexible part-time schedule
  • Opportunity to contribute to cutting-edge clinical research and expand expertise in dermatology

For more information reach out Asra Moosvi at (469) 290 - 0934 / asra.moosvi@protouchstaffing.com

Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

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