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Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

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 ...

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As of Jun 10, 2026, the average hourly pay for from home icon cra in the United States is $36.02, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $31.01 per hour, depending on experience, location, and employer.

What are some common challenges faced by remote Clinical Research Associates (CRAs) and how can they be addressed?

Remote Clinical Research Associates often face challenges such as coordinating with on-site teams, maintaining effective communication, and ensuring regulatory compliance from a distance. Utilizing project management tools and regularly scheduled video conferences can help streamline collaboration and maintain oversight. Additionally, staying organized and proactive in follow-ups ensures data integrity and regulatory standards are upheld. Building strong relationships with site staff and leveraging technology are key to overcoming these remote work challenges.

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From Home Icon Crafters are professionals who design and create digital icons while working remotely, typically from their own homes. They use graphic design software to produce icons for websites, apps, user interfaces, and branding materials. This role requires creativity, attention to detail, and proficiency in design tools such as Adobe Illustrator or Figma. Working from home allows for flexible hours and the ability to collaborate with clients or teams online.

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Common Search IntentIcon creation, graphic design from homeIcon creation, graphic design from home

The comparison shows that From Home Icon Cra and From Home Icon Cra are essentially the same role, focusing on creating icons remotely within the digital design industry. Both require similar skills and are used interchangeably in job searches related to remote icon design tasks.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA) working from home, and why are they important?

To thrive as a remote Clinical Research Associate (CRA), you need a solid understanding of clinical trial protocols, regulatory guidelines, and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as ACRP or SOCRA are highly valued. Strong organizational skills, attention to detail, and effective virtual communication set top performers apart in this role. These competencies are crucial to ensure regulatory compliance, maintain data integrity, and successfully manage study sites from a remote environment.
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Senior Clinical Research Associate

Senior Clinical Research Associate

Icon plc

Cary, NC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 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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