ICON plc·Washington, District of Columbia
The Senior CRA is responsible for managing investigative sites and performing monitoring visits to ensure data integrity and subject safety in Oncology clinical trials. This includes facilitating communication between the client and sites, managing essential documents, and ensuring inspection readiness.
Senior Clinical Research Associate - Oncology - Washington DC
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.
The Sr.
Clinical Research Associate (Sr.
CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle.
This Sr.
CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
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
Candidates must have a bachelor's degree and over 5 years of independent clinical trial monitoring experience, including at least 2 years in solid tumor trials. Proficiency in GxPs, Oncology monitoring techniques, and experience with Veeva systems is highly preferred.
Market context
In the District of Columbia, Senior Clinical Research Associate roles are typically driven by ongoing oncology and clinical trial activity, with employers looking for experienced monitors who can work independently. This role is competitive because it requires a bachelor’s degree, over 5 years of monitoring experience, and at least 2 years in solid tumor trials, with GxPs, oncology monitoring, and Veeva experience preferred. Review the AI-summarized requirements and benefits here to save research time, then tailor your application to highlight trial types, monitoring scope, and systems experience.