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Icon Plc Jobs in Raleigh, NC (NOW HIRING)

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

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 ...

Icon plc

Project Manager II, Laboratory

Raleigh, NC · Hybrid

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 ...

Icon plc

Medical Director (Endocrinology)

Raleigh, NC · Remote

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 ...

Icon plc

Site Management Associate I

Raleigh, NC · On-site

Site Management Associate I 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 ...

Icon plc

Patient Recruitment Lead

Raleigh, NC · On-site

Patient Recruitment Lead 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 ...

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How much do icon plc jobs pay per hour?

As of Jul 14, 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.

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What cities near Raleigh, NC are hiring for Icon Plc jobs? Cities near Raleigh, NC with the most Icon Plc job openings:
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Infographic showing various Icon Plc job openings in Raleigh, NC as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $68,329 per year, or $32.9 per hour.
Senior Clinical Research Associate

Senior Clinical Research Associate

Icon plc

Cary, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 17 days ago

Job description

Senior CRA / CRA II - Home-Based (US)

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 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%)

    #LI-LB1 #LI-REMOTE


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 requesthere.

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

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