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Clinical Trial Risk Based Monitoring Jobs in Raleigh, NC

ICON

Country Lead Monitor

Raleigh, NC · On-site

... trial design, vendor selection, and risk management. Your Profile: You will have solid clinical ... Prior monitoring experience is preferred * Willingness to travel as required (approximately 25 ...

Icon plc

Country Lead Monitor

Raleigh, NC · On-site

... trial design, vendor selection, and risk management. Your Profile: You will have solid clinical ... Prior monitoring experience is preferred * Willingness to travel as required (approximately 25 ...

ICON

Country Lead Monitor

Raleigh, NC · On-site

... trial design, vendor selection, and risk management. Your Profile: You will have solid clinical ... Prior monitoring experience is preferred * Willingness to travel as required (approximately 25 ...

ICON

Country Lead Monitor

Raleigh, NC · On-site

... trial design, vendor selection, and risk management. Your Profile: You will have solid clinical ... Prior monitoring experience is preferred * Willingness to travel as required (approximately 25 ...

ICON

Country Lead Monitor

Raleigh, NC · On-site

... trial design, vendor selection, and risk management. Your Profile: You will have solid clinical ... Prior monitoring experience is preferred * Willingness to travel as required (approximately 25 ...

Icon plc

Clinical Research Associate II

Cary, NC · Remote

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package ...

Icon plc

Clinical Research Associate II

Raleigh, NC · Remote

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package ...

Icon plc

Clinical Research Associate II

Raleigh, NC · Remote

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package ...

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Clinical Trial Risk Based Monitoring information

See Raleigh, NC salary details

$16

$38

$68

How much do clinical trial risk based monitoring jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical trial risk based monitoring in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.

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 Raleigh, NC?

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

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

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities near Raleigh, NC 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 Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $80,847 per year, or $38.9 per hour.

Country Lead Monitor

ICON

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Country Lead Monitor
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
What You Will Do:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Your Profile:
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
  • University degree in medicine, science, or equivalent combination of education & experience
  • Demonstrated ability to drive the clinical deliverables of a study
  • Subject matter expertise in the designated therapeutic area
  • Prior monitoring experience is preferred
  • Willingness to travel as required (approximately 25%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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