ICON plc·Chicago, Illinois
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing site documentation, and overseeing drug accountability throughout the clinical trial process.
Clinical Research Associate - Oncology - Chicago
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.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
may vary depending on role and location.
Visit our careers site [https://careers.iconplc.com/benefits] to read more about the benefits ICON offers.
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.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here [https://careers.iconplc.com/reasonable-accommodations].
$91,336.00-$114,170.00
Are you a current ICON Employee? Please click here [https://wd3.myworkday.com/icon/d/task/1422$1235.htmld] to apply
Candidates must have a Bachelor’s degree in Life Sciences or be a qualified RN, with at least 2 years of on-site monitoring experience in the pharmaceutical or CRO industry. Proficiency in Oncology clinical trials and familiarity with clinical systems like CTMS and eTMF are required.
Market context
Clinical Research Associate II openings in Illinois are often driven by ongoing pharmaceutical and CRO trial activity, especially in oncology. These roles are competitive because employers usually want a Life Sciences degree or RN background, at least 2 years of on-site monitoring experience, and comfort with CTMS and eTMF systems. If you are considering applying, quickly map your oncology monitoring experience to the posting and note that the job requirements and benefits here are AI-summarized from the original description, saving research time.
