Clinical Research Associate - Oncology - Central / Eastern Region (Field Based)

Clinical Research Associate - Oncology - Midwest / Eastern Region (Field Based)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing :

Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines.

Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and closes clinical trials at investigative sites.

Responsible for site startup activities for assigned sites, including but not limited to regulatory documents collection, informed consent review, IRB / IEC submission support, and budgets and contracts negotiations.

Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely

Provides regular site status information to team members, trial management, and updates trial management tools.

Completes monitoring activity documents as required by sponsor's SOPs.

Works closely with other clinical team members to facilitate timely resolution of trial and / or clinical issues.

Escalates site and trial related issues per Sponsor's SOPs until identified issues are resolved or closed.

Performs essential document site file reconciliation.

Performs source document verification and query resolution.

Assesses investigational product (IP) accountability, dispensation, and compliance at the investigative sites.

Verifies serious adverse event (SAE) reporting according to trial specifications and ICH GCP guidelines.

Communicates with investigative sites.

Updates applicable tracking systems

Ensures all required training is completed and documented.

May be assigned to complex studies and / or sites.

Provides leadership skills to assigned projects within the clinical operations department.

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 2-3 years of clinical monitoring experience, including at least 1 year of on-site monitoring (vs all remote monitoring)

Located in the Central or Eastern region near a major hub, with the ability to travel up to 50% of the time (remote and on site visits)

1 year Oncology experience strongly preferred; nephrology, hematology, immunology also acceptable

(If no oncology experience, startup experience 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

Pay Range ($91,336.00 / Yr.USD - 114,170.00 / Yr USD)

• Actual compensation will be determined based on factors such as geographic location, work experience, education / training, and skill level.

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 site to read more about the benefits ICON offers.

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, color, 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 or submit a request here

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.

Are you a current ICON Employee? Please click here to apply