As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
ResponsibilitiesWhat You Will Be Doing:
Conducting qualification, initiation, monitoring, and close-out visits in accordance with study protocols and ICH-GCP guidelinesEnsuring the rights, safety, and well-being of study participants are protectedVerifying the accuracy and completeness of data collected at investigative sitesCollaborating closely with site staff and cross-functional teams to proactively identify and resolve study-related issuesEnsuring all study documentation is accurate, up-to-date, and audit-readyProviding training and support to site personnel on study procedures and regulatory requirementsMonitoring complex Phase 1 oncology trials, which may include dose-escalation, first-in-human, and combination therapy protocolsThis is a high-impact role ideal for professionals with strong clinical monitoring skills, a keen eye for detail, and a passion for advancing oncology research at the forefront of innovation. Qualifications
You Are:
A dedicated clinical research professional with an undergraduate degree in a clinical, scientific, or health-related field from an accredited institution — or equivalent relevant experience. A licensed healthcare professional (e.g., RN) is also acceptable.
An experienced Clinical Research Associate with 5+ years of clinical monitoring experience, including at least 1-2 years of on-site monitoring
Located in the northeast region with the ability to travel up to 50% of the time
Experienced in oncology trials; SCLC or NSCLC experience preferred but not required
Proficient in feasibility assessments, site selection, and site start-up activities
Familiar with or experienced in Phase 1 dose escalation studies (preferred)
Comfortable supporting budget negotiations and resolving site-level challenges (preferred)
Highly proactive, detail-oriented, and collaborative — a team player who takes initiative and communicates effectively
Well-versed in ICH-GCP guidelines and applicable local regulatory requirements
Able to lead observation and performance monitoring visits and act as a resource across functional teams to ensure study progress
Skilled in managing tasks that require advanced negotiation and problem-solving
Fluent in spoken and written English
Legally authorized to work in the United States without requiring current or future employment visa sponsorship
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.