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Icon Plc Jobs in Raleigh, NC (NOW HIRING)

Sr. 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 ...

Sr. 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 ...

Sr. 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 ...

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 ...

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 ...

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 ...

Country Lead Monitor 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 ...

Country Lead Monitor 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 ...

Lead CRA - Ophthalmology 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 ...

Country Lead Monitor 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 ...

Country Lead Monitor 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 ...

Project Manager, II Labs- hybrid 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 ...

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 ...

Clinical Research Coordinator Nurse - Raleigh, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Clinical Research Coordinator Nurse - Raleigh, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Medical Director (Endocrinology/Obesity)- United States- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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Icon Plc information

See Raleigh, NC salary details

$19

$32

$41

How much do icon plc jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for icon plc in Raleigh, NC is $32.85, according to ZipRecruiter salary data. Most workers in this role earn between $29.42 and $36.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at ICON plc, and why are they important?

To thrive as a Clinical Research Associate at ICON plc, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for success in this role. These skills and qualifications are vital to ensuring clinical trials are conducted accurately, ethically, and in compliance with regulatory standards.

What is ICON plc and what does the company do?

ICON plc is a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. The company specializes in clinical research and provides a wide range of services including clinical trial management, consulting, and laboratory services. ICON plc helps organizations bring new medicines and medical devices to market by managing and conducting clinical studies and ensuring regulatory compliance. Founded in 1990 and headquartered in Dublin, Ireland, ICON operates in over 40 countries worldwide.

What are some typical responsibilities for a Clinical Research Associate at ICON Plc, and how does the role contribute to successful clinical trials?

As a Clinical Research Associate (CRA) at ICON Plc, your primary responsibilities include monitoring clinical trial sites, ensuring compliance with study protocols, and maintaining accurate documentation. You'll frequently collaborate with site staff and cross-functional teams to resolve any issues and support patient safety and data integrity. The role requires regular travel to trial locations, attention to regulatory requirements, and effective communication skills. Your contributions are vital for keeping studies on track and ensuring high-quality, reliable results for sponsors.

What is the difference between Icon Plc vs Clinical Research Associate?

AspectIcon PlcClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or CRA are commonRequires similar degrees; certifications like CCRA or CRA are often necessary
Work EnvironmentGlobal clinical trial sites, offices, and remote settingsMonitoring clinical trials at sites, coordinating with sponsors and sites
Employer & Industry UsageContract research organization (CRO) providing clinical trial servicesRole within CROs, pharmaceutical companies, or biotech firms

Icon Plc is a leading CRO that employs Clinical Research Associates (CRAs) to monitor and manage clinical trials. Both roles require similar qualifications and work in comparable environments, often within the pharmaceutical and biotech industries. The main difference lies in the company branding and specific project assignments, but their responsibilities and credentials overlap significantly.

What cities near Raleigh, NC are hiring for Icon Plc jobs? Cities near Raleigh, NC with the most Icon Plc job openings:
Infographic showing various Icon Plc job openings in Raleigh, NC as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $68,325 per year, or $32.8 per hour.
Sr. Clinical Research Associate

Sr. Clinical Research Associate

Icon plc

Raleigh, NC โ€ข On-site

Full-time

Medical, Life, Retirement, PTO

Posted 8 days ago


Job description

Sr. 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