CRA II

ICON Strategic Solutions; North Carolina; On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II for Southeast territory in the United States. The role focuses on monitoring and data quality across sponsor-dedicated trials, contributing to patient safety and regulatory compliance.

You will perform site qualification through close-out visits, coordinate with investigators, review data, and help prepare essential trial documents while traveling about 60% of the time.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• 2+ years of experience as a Clinical Research Associate.
• Solid knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Responsibilities

• Conduct site qualification, initiation, monitoring and close-out visits.
• Ensure protocol compliance, data integrity and patient safety.
• Collaborate with investigators and site staff to support study conduct.
• Perform data review and resolve queries to maintain high-quality data.
• Prepare and review study documentation including protocols and reports.

Skills

Clinical trial monitoring

ICH-GCP knowledge

Documentation

Communication

Team collaboration

Travel willingness

Education

Bachelor's degree in science/healthcare

Job description

Clinical Research Associate II- Southeast

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a CRA II at ICON, you will design and analyse 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 scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• 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.
• Willingness to travel as required (approximately 60%)

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

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