Senior Clinical Research Associate

ICON Clinical Research; Cincinnati (OH); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Global EAP LifeWorks

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (Oncology) in Ohio. The role focuses on serving as the primary site sponsor liaison, conducting site visits, and ensuring regulatory compliance across multiple therapeutic areas.

You will manage CTMS/eTMF documentation, support training, and monitor safety with regional travel up to 50%. The ideal candidate holds a Life Sciences degree or RN qualification and has 2+ years of on-site monitoring experience in pharma or CRO

Qualifications

• Bachelor’s degree in Life Sciences or RN qualification is required.
• Eligible to work in the United States without visa sponsorship.
• 2+ years of on-site monitoring experience in pharma or CRO.
• Experience in Oncology and multiple therapeutic areas is preferred.

Responsibilities

• Serve as the primary contact between sites and sponsor.
• Conduct site visits: selection, initiation, monitoring, close-out.
• Ensure ICH-GCP and regulatory compliance.
• Maintain documentation in CTMS and eTMF systems.
• Support site staff training and compliance records.
• Monitor safety and AE/SAE reporting; support recruitment.

Skills

On-site monitoring

Clinical research

ICH-GCP

CTMS

eTMF

Travel up to 50%

Education

Bachelor’s degree in Life Sciences

RN qualification

Tools

CTMS

eTMF

Job description

Senior Clinical Research Associate - Oncology - Ohio

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

What You Will Be Doing:

• Serve as the primary point of contact between investigational sites and the sponsor

• Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

• Ensure site compliance with ICH-GCP, SOPs, and regulations

• Maintain up-to-date documentation in CTMS and eTMF systems

• Support and track site staff training and maintain compliance records

• Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

• Support subject recruitment and retention efforts at the site level

• Oversee drug accountability and ensure proper storage, return, or destruction

• Resolve data queries and drive timely, high-quality data entry

• Document site progress and elevate risks or issues to the clinical team

• Assist in tracking site budgets and ensuring timely site payments (as applicable)

• Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

• A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN

• Eligible to work in United States without visa sponsorship

• A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

• Experienced across multiple therapeutic areas, ideally including Oncology (Prostate Cancer, and Lung Cancer) and Hematology

• Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

• A clear communicator, problem-solver, and collaborative team player

• Willing and able to travel up to 50% for on-site monitoring visits across northeast region; preference given to candidates residing in Cincinnati, OH near major HUB airports to support efficient regional travel

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:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family’s needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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 (https://careers.iconplc.com/reasonable-accommodations)