ICON plc·Phoenix, Arizona
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and driving high-quality data entry.
Senior Clinical Research Associate - Oncology - West Region
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].
$110,520.00-$138,150.00
Are you a current ICON Employee? Please click here [https://wd3.myworkday.com/icon/d/task/1422$1235.htmld] to apply
Requires a Bachelor's degree in Life Sciences or RN qualification and at least 3 years of on-site monitoring experience in pharmaceutical or CRO industries. Candidates must have specific experience in Oncology or Hematology Oncology trials and be able to travel up to 50%.
Market context
In Arizona, Senior Clinical Research Associate openings are typically driven by ongoing oncology and hematology oncology trial activity, with employers looking for candidates who can handle frequent site monitoring and travel. This role is competitive because it requires a life sciences degree or RN qualification, at least 3 years of on-site monitoring experience in pharma or CRO settings, and therapeutic-area experience that is not easy to substitute. Review the AI-summarized requirements and benefits here to save research time, then confirm your oncology monitoring history and travel availability before applying.