ICON plc·Florida
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and regulations. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data quality and site documentation.
Clinical Research Associate - Oncology - West Palm Beach, FL
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].
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 and at least 2 years of on-site monitoring experience in the pharmaceutical or CRO industry. Candidates must have specific experience in Oncology or Hematology Oncology studies and be willing to travel up to 50%.
Market context
In Florida, Clinical Research Associate II openings often reflect steady demand from pharmaceutical and CRO teams running oncology and hematology oncology studies. These roles are competitive because employers usually want a life sciences degree or RN background, at least 2 years of on-site monitoring experience, and willingness to travel up to 50%. Review the oncology study details closely and tailor your application to show relevant monitoring sites, travel readiness, and clinical research experience; this platform’s AI-summarized requirements and benefits from the original posting can save you time during that review.