ICON plc·Washington, District of Columbia
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for oncology clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
Clinical Research Associate - West Coast 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.
As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. Our FSP program is looking for an Oncology monitor in on the West Coast. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Bachelor's degree in a scientific or healthcare-related field. Oncology monitoring experience Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%)
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 include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways
may vary depending on role and location.
Visit our careers site 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.
$91,336.00-$114,170.00 Are you a current ICON Employee? Please click here to apply
Candidates must have a bachelor's degree in a scientific or healthcare field and at least 2 years of experience as a CRA with specific oncology monitoring expertise. In-depth knowledge of ICH-GCP guidelines and a willingness to travel approximately 60% are required.
Market context
Clinical Research Associate roles in the District of Columbia often reflect steady demand from sponsors, CROs, and research organizations tied to the region’s life sciences and healthcare ecosystem. This role is competitive because employers want oncology monitoring experience, strong ICH-GCP knowledge, and willingness to travel; the posted requirements and benefits are AI-summarized from the original job description, saving you research time. If you are applying, highlight oncology site-monitoring examples and confirm your travel flexibility early.
