ICON plc·New York
Perform comprehensive site management and monitoring activities for oncology clinical trials to ensure data integrity and subject safety. Act as the primary liaison between the client's trial team and sites while maintaining inspection readiness and compliance with protocols.
Senior Clinical Research Associate - Oncology - New York
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 and over 5 years of independent clinical trial monitoring experience, including at least 2 years in solid tumor trials. Candidates must be proficient in GxPs and willing to travel up to 50%.
Market context
Senior Clinical Research Associate roles in New York are typically driven by ongoing clinical trial activity across sponsors, CROs, and research sites, with strong demand for monitors who can work independently. This role is competitive because it requires a bachelor’s degree, 5+ years of monitoring experience, at least 2 years in solid tumor trials, GxP proficiency, and travel up to 50%. Before applying, compare your oncology monitoring background and travel readiness to the posting; job requirements and benefits here are AI-summarized from the original job description, saving you research time.
