Clinical Research Associate (East Coast)

ICON; United States; Remote; USD 65,000 - 90,000; Full time

Job summary

As a Clinical Research Associate at a leading company, you will monitor and ensure the success of clinical trials. Your role involves managing site visits, maintaining protocol compliance, and collaborating with study staff. ICON values a diverse work culture and offers competitive benefits focused on well-being and performance.

Benefits

Various annual leave entitlements

A range of health insurance options for you and your family

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate with on-site monitoring experience.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

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 smooth study conduct.

Skills

Organizational skills

Communication skills

Attention to detail

Education

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

Job description

As a CRA, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• 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.

You are:

• Bachelor's degree in a scientific or healthcare-related field is highly preferred.
• Minimum of 2 years of experience as a Clinical Research Associate with on-site monitoring experience required.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.

What ICON can offer you:

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• A range of health insurance options for you and your family
• Competitive retirement planning to maximize savings
• Global Employee Assistance Programme, TELUS Health, providing 24/7 support from over 80,000 professionals
• Life assurance
• Flexible country-specific benefits such as childcare vouchers, bike schemes, gym memberships, travel passes, health assessments, etc.

Visit our careers website to learn more about working at ICON.

At ICON, inclusion & belonging are core to our culture. We are committed to providing an inclusive environment free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, religion, gender, sexual orientation, or other protected characteristics. If you need accommodations during the application process, please let us know through the reasonable accommodations form.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for, whether for this or other roles.