Senior Clinical Research Associate
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Job overview
ICON Clinical Research is seeking a Senior Clinical Research Associate or Clinical Research Associate II to support clinical trials. The role conducts site visits, ensures protocol compliance and patient safety, collaborates with investigators and site staff, reviews data, resolves queries, and contributes to study documentation. Candidates need a scientific or health-related degree or equivalent education and clinical research experience, and must be able to travel at least 60% of the time.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Senior CRA - Home-Based (US)
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
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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
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Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
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Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior 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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Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
#LI-KC2 #LI-REMOTE
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
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