CRA II
Remote · USJobSeen 1w agoSeen in employer's feed 2 days ago
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Requirements
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Job overview
At ICON Strategic Solutions, the CRA II works in a sponsor-dedicated model supported by ICON’s global expertise. The role contributes to clinical trial monitoring and involves site visits, protocol compliance, data review, and collaboration with investigators and site staff. The position requires a scientific or healthcare-related bachelor’s degree, at least two years of CRA experience, and willingness to travel approximately 60%.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Clinical Research Associate
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:
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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
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
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Bachelor's degree in a scientific or healthcare-related field.
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Minimum of 2 years of experience as a Clinical Research Associate.
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In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
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Strong organizational and communication skills, with attention to detail.
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Ability to work independently and collaboratively in a fast-paced environment.
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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:
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Various annual leave entitlements
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A range of health insurance offerings to suit you and your family’s needs.
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Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
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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.
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Life assurance
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Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
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 (https://careers.iconplc.com/reasonable-accommodations)
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
How this job compares
Set against the 449 open Clinical Research Associate jobs on Olive Jobs, counted November 13, 2026.
- Pay
- This postingNot listed
- US median$75–175K/yr226 salary ranges
- US median$58–62/hr41 hourly ranges
- Openings
- Olive Jobs lists 449 open Clinical Research Associate jobs across the US. 26% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- IQVIA142 open
- Parexel105 open
- ThermoFisher Scientific68 open
- Experience
- This posting asks for at least 2 years of experience; Clinical Research Associate postings that state a minimum ask for 2 years at the median (403 postings).
- Education
- This posting asks for a bachelor's degree; 85 of the 449 open Clinical Research Associate jobs (19%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 13, 2026. Figures based on too few postings are left out.
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