ICON plc·San Diego, California
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
Senior Clinical Research Associate - Oncology - Southern California
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 Veeva systems and expertise in GxP and Oncology monitoring techniques are highly preferred.
Market context
Senior Clinical Research Associate roles in California are typically driven by sustained demand for experienced oncology monitors, especially in solid tumor studies. This category is competitive because employers often look for independent trial monitoring experience, Veeva proficiency, and strong GxP knowledge, with oncology-specific expertise setting candidates apart. If you are considering applying, align your resume to solid tumor monitoring work and note that the job requirements and benefits here are AI-summarized from the original description, which can save time during your search.
