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About the Role

ICON is a global healthcare intelligence and clinical research organisation focused on accelerating the delivery of new medicines and treatments to patients. We are a values-driven company committed to integrity, collaboration, agility, and inclusion.

Responsibilities

• 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 CTMs.

Requirements

• Eligible to work in United States without visa sponsorship.
• A 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 eTMF.
• A clear communicator, problem-solver, and collaborative team player.
• Willing and able to travel up to 50% for on-site monitoring visits across the East 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.

Skills

• ICH-GCP
• CTMS
• eTMF

Location

• East Region

Work Type

• On-site monitoring
• Travel up to 50%

Experience Level

• Senior
• 3+ years of on-site monitoring experience

Education Level

• Bachelor’s degree in Life Sciences or equivalent
• Qualified RN

Salary/Compensations

• $110,520.00-$138,150.00

Benefits

• 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

About the Company

• 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.
• ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide.
• You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.

Equal Opportunity

• 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.