CRA III Job at ICON Strategic Solutions, Las Vegas, NV

  • ICON Strategic Solutions
  • Las Vegas, NV

Job Description

Job Description

Clinical Research Associate - Las Vegas, NV

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ICON is a global healthcare intelligence and clinical research organization united by a mission to bring new medicines and treatments to patients faster.

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As a values-driven organization, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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As a CRA at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

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What You Will Do:

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You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

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Key responsibilities include:

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  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
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  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
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  • Collaborating with investigators and site staff to facilitate smooth study conduct.
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  • Performing data review and resolution of queries to maintain high-quality clinical data.
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  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
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Your Profile:

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You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

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Required qualifications and experience:

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

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Rewards & Benefits

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ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

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Benefits may include:

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  • Competitive base salary and performance related incentives
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  • Health and wellbeing programs including medical, dental, and vision coverage where applicable
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  • Retirement and pension plans
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  • Life assurance and disability coverage
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  • Employee assistance programs and wellbeing resources
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  • Learning and development opportunities through structured training and career pathways
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Benefits may vary depending on role and location.

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

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Inclusion and Accessibility

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ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

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