ICON plc·New York
Serve as the primary contact between investigational sites and the sponsor 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 (Myelofibrosis) - East 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 an RN qualification with over 3 years of on-site monitoring experience in pharmaceutical or CRO industries. Specific experience monitoring Oncology (Myelofibrosis) trials and the ability to travel up to 50% is essential.
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.