ICON plc·Texas
Serve as the primary contact between investigational sites and the sponsor while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Oversee patient safety reporting, drug accountability, and high-quality data entry within CTMS and eTMF systems.
Senior Clinical Research Associate - Oncology/Myelofibrosis - Central 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 RN qualification and at least 3 years of on-site monitoring experience in pharma or CRO. Must have specific experience monitoring Oncology/Myelofibrosis trials and be able to travel up to 50% within the Central region.
Market context
In Texas, Senior Clinical Research Associate roles are typically driven by ongoing demand for experienced monitors who can support oncology studies and regional site activity. These positions are competitive because employers often want a life sciences degree or RN background, at least 3 years of on-site monitoring experience, and direct Oncology/Myelofibrosis trial experience, plus the ability to travel up to 50% in the Central region. Review the AI-summarized requirements and benefits here to save research time, then tailor your application to highlight oncology monitoring and travel readiness.