CRA III

ICON Strategic Solutions; Las Vegas (NV); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive base salary

Comprehensive health programs

Retirement and pension plans

Life insurance

Wellbeing resources

Learning and development opportunities

Job summary

ICON is hiring a Clinical Research Associate for the Las Vegas, NV area to design and monitor clinical trials, focusing on cardiology studies and data integrity. Travel of about 60% is expected to manage multiple sites and ensure patient safety and protocol adherence.

You will collaborate with investigators, review data, and contribute to study documentation while advancing regulatory compliance and high-quality trial conduct.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Cardiology Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Cardiology experience required, Med Device experience preferred.
• 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%)

Responsibilities

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

Skills

Clinical trial monitoring

Regulatory knowledge

Cardiology expertise

Data integrity

Site management

Communication

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Job description

Clinical Research Associate - Las Vegas, NV

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

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.

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.

What You Will Do:

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

Key responsibilities include:

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

Your Profile:

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

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Cardiology Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Cardiology experience required, Med Device experience preferred
• 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%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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 programs including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programs and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

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.