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Clinical Trial Risk Based Monitoring Jobs in Colorado

ECN Operating LLC

Clinical Research Coordinator

Denver, CO

$25 - $33.25/hr

Communicate with sponsors, monitors, and IRBs regarding study progress and compliance. * Schedule ... Familiarity with IRB processes and clinical trial documentation. * Bilingual skills (depending on ...

Denver Health

Senior Clinical Risk Manager

Denver, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Risk Manager works closely with senior leadership, participates in ... Participate in early resolution, mediations, settlements and/or trial, and ensure compliance with ...

Denver Health

Senior Clinical Risk Manager

Denver, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Participate in early resolution, mediations, settlements and/or trial, and ensure compliance with ... based health centers, Rocky Mountain Poison & Drug Safety, the Public Health Institute at Denver ...

CPC

Sr. Clinical Operations Manager

Aurora, CO · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Review and finalize monitoring visit reports and follow-up letters with Clinical Research ... Oversee trial-related activities and provide performance feedback to supervisors for all project ...

HCA HealthONE Rose

Clinical Dietitian PRN

Denver, CO · On-site

Identify patients at nutritional risk based on established criteria * Evaluate age specific ... Evaluate and monitor the effectiveness and outcomes of medical nutrition therapy interventions.

FINRA

Principal Analyst, Risk Monitoring

Denver, CO · Hybrid

$112K - $211K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

What You'll Do * Lead risk monitoring activities for complex and elevated-risk member firms ... In addition to location, actual compensation is based on various factors, including but not limited ...

Nira Medical

Prepare, submit, and manage sponsor invoices based on executed clinical trial agreements, study budgets, payment milestones, and contractual terms. * Monitor accounts receivable and proactively ...

CU Denver

Clinical Research Professional (Open Rank)

Aurora, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Schedule subject participation in research clinical trial, coordinating availability of necessary ... The duties of this position may change from time to time and/or based on business need. We reserve ...

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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 Colorado?

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

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

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

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

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

Clinical Trial Risk Based Monitoring jobs near you

Clinical Research Psychiatrist - Denver, CO

ProTouch Staffing

Denver, CO

Other

Re-posted 27 days ago

Job description

Part-Time Psychiatrist

 Denver, CO | ⏰ Part-Time (0-8 hours/week)

About the Role

We are seeking a Board-Certified Physician to join as a Clinical Research Physician supporting Phase I-IV clinical trials in Denver, CO . In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies.

Key Responsibilities

  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.

  • Conduct medical screenings, physical exams, and assessments of study participants.

  • Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.

  • Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.

  • Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.

  • Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.

  • Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.

  • Contribute to feasibility reviews, study design, and recruitment strategies.

  • Stay current with clinical research regulations and therapeutic advances.

Qualifications

  • M.D. or D.O. with an active, unrestricted Illinois medical license.

  • Board Certification in Psychiatry.

  • Valid DEA license and BLS/ACLS certification.

  • Clinical research/clinical trials experience preferred (training available for motivated candidates).

  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).

  • Excellent communication, collaboration, and interpersonal skills.

  • Strong commitment to ethical research and patient-centered care.

Benefits

  • Flexible, part-time schedule (0-8 hours per week).

  • Opportunity to expand expertise in multi-therapeutic clinical trials.

  • Direct involvement in advancing innovative treatments through research.

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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