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    Job · 14442027

    ICON Strategic Solutions logo

    Clinical Research Associate

    ICON Strategic Solutions · Remote · remote · Posted 55d ago

    Not disclosed2+ yrsfulltimeSourced fromWorkday

    About a minute. You'll make an account on the way through.

    About this role

    Clinical Research Associate - Early Development Multi Therapeutic - Regional (major hubs) 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 investigation sites and the sponsor for early development multi therapeutic clinical trials.

    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

    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 monitoring early development Phase I/II clinical studies, across multiple therapeutic areas

    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 60% for on-site monitoring visits; preference given to candidates residing near major HUB airports 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 .

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

    Sourced from workday

    Skills

    google cloud platform

    About ICON Strategic Solutions

    ICON Strategic Solutions logo

    ICON Strategic Solutions

    1990

    36 years old

    Dublin

    IE

    About

    ICON is a global provider of outsourced drug development services to biopharma, medical device, biosimilar and generic organizations. ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I-IV clinical studies.

    Industries

    BiopharmaBiotechnologyMedicalPharmaceutical

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