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Icon Clinical Research Cra Jobs (NOW HIRING)

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Clinical Research Associate II

Charlotte, NC · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Mcfarland, CA · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Lawrence, KS · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Portland, OR · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Bristol, TN · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Clinical Research Associate II

Boston, MA · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data ...

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Clinical Research Administrator

Lisle, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

Clinical Research Assoicate ICON is a global healthcare intelligence and clinical research ... As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data ...

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Clinical Research Administrator

Oak Lawn, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

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Clinical Research Administrator

Winfield, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

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Clinical Research Associate

Indianapolis, IN · On-site

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data ...

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Clinical Research Associate

Blue Bell, PA · On-site

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data ...

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All JobsIcon Clinical Research Cra Jobs

Icon Clinical Research Cra information

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$11K

$79.4K

$137.5K

How much do icon clinical research cra jobs pay per year?

As of Sep 9, 2026, the average yearly pay for icon clinical research cra in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What does a Clinical Research Associate at ICON Clinical Research do?

A Clinical Research Associate (CRA) at ICON Clinical Research is responsible for monitoring clinical trials to ensure they are conducted following regulatory requirements and study protocols. CRAs act as the main point of contact between the sponsor and research sites, verifying data accuracy, ensuring participant safety, and conducting site visits. Their work is crucial in maintaining the integrity of clinical data and supporting the successful completion of clinical studies.

What are some common challenges faced by Clinical Research Associates at ICON, and how can applicants prepare for them?

Clinical Research Associates at ICON often manage multiple trials across various sites, which requires strong organizational skills and adaptability. Common challenges include ensuring compliance with complex regulatory requirements, maintaining clear communication with site staff, and managing travel schedules. Applicants can prepare by developing meticulous attention to detail, honing their time management abilities, and familiarizing themselves with Good Clinical Practice (GCP) guidelines. Building a proactive approach to problem-solving and fostering collaborative relationships with colleagues can also help navigate these challenges successfully.

What are the key skills and qualifications needed to thrive as an ICON Clinical Research CRA, and why are they important?

To thrive as an ICON Clinical Research CRA (Clinical Research Associate), you need a solid background in life sciences, clinical research processes, and regulatory guidelines, typically supported by a relevant degree and prior monitoring experience. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are commonly required. Strong organizational skills, attention to detail, and effective communication make candidates excel in this role. These competencies are crucial for ensuring compliance, data integrity, and successful collaboration in complex clinical trials.

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

AspectIcon Clinical Research CraClinical Research Associate
CertificationsTypically requires GCP training, CRA certificationRequires GCP training, often CRA certification
Work EnvironmentPharmaceutical/clinical research companies, CROsPharmaceutical companies, CROs, research sites
Employer & IndustryMajor CROs like Icon, industry-widePharmaceutical companies, CROs, industry-wide
Search & Comparison IntentIcon Clinical Research Cra vs Clinical Research AssociateSame as above

The main difference between an Icon Clinical Research Cra and a Clinical Research Associate is primarily in branding and company affiliation. Both roles involve monitoring clinical trials, ensuring compliance, and working within similar environments. The titles are often used interchangeably, but 'Icon Clinical Research Cra' specifies employment with Icon, a leading CRO, while 'Clinical Research Associate' is a broader industry term applicable across many organizations.

What are popular job titles related to Icon Clinical Research Cra jobs?

For Icon Clinical Research Cra jobs, the most frequently searched job titles are:

Infographic showing various Icon Clinical Research Cra job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate II

Charlotte, NC • Remote

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See more jobs at Icon plcexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 19 days ago

Job description

Senior CRA / CRA II - United States - Home Based

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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