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Clinical Trial Risk Based Monitoring Jobs in Raleigh, NC

Icon plc

Sr. Clinical Research Associate

Durham, NC · On-site

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. * Conducting site visits to assess site performance ...

IQVIA

Clinical Lead

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

IQVIA

Clinical Lead

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

IQVIA

Clinical Lead

Durham, NC

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

IQVIA

Clinical Lead

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

IQVIA

Clinical Supply Chain Manager

Durham, NC · On-site

$68.40K - $171K/yr

... monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems ... Clinical Trial Supplies team Conducts thorough and regular risk management assessments to ensure ...

IQVIA, Inc.

Clinical Supply Chain Manager

Durham, NC · On-site

$68.40K - $171K/yr

... monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems ... the IQVIA Clinical Trial Supplies team • Conducts thorough and regular risk management ...

IQVIA

Clinical Supply Chain Manager

Durham, NC · On-site

$68.40K - $171K/yr

... monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems ... Clinical Trial Supplies team Conducts thorough and regular risk management assessments to ensure ...

IQVIA, Inc.

Clinical Lead

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

IQVIA, Inc.

Clinical Lead

Durham, NC · On-site

Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

IQVIA

Associate Clinical Lead Director

Durham, NC · On-site

Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional ...

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Clinical Trial Risk Based Monitoring information

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$38

$68

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

As of May 28, 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 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.

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 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.

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 May 2026, with employment types broken down into 4% As Needed, 80% Full Time, 6% Part Time, 2% Temporary, 7% Contract, and 1% Nights. Highlights an 91% Physical, 6% Hybrid, and 3% Remote job distribution, with an average salary of $80,847 per year, or $38.9 per hour.
Sr. Clinical Research Associate

Sr. Clinical Research Associate

Icon plc

Raleigh, NC

Full-time

Medical, Life, Retirement, PTO

Posted 19 days ago

Job description

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family's needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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