Senior Clinical Research Associate

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.

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 escalate 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 CTMsYou 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 sponsorshipA clinical research professional with 3+ years of on-site monitoring experience in the pharmaceutical or CRO industry

Experienced monitoring Oncology specifically Myelofibrosis clinical trials.

Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMFA clear communicator, problem-solver, and collaborative team player

Willing and able to travel up to 50% for on-site monitoring visits across the Central region; preference given to candidates residing near major HUB airport to support efficient regional travel

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.

Benefits 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

Benefits 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.

Salary Range$-$Are you a current ICON Employee? Please  to apply

Summary

Location:

Texas;
Michigan;
Nebraska;
Tennessee;
Wisconsin;
Kentucky;
Illinois;
Missouri Type:
Full time