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    • Senior Clinical Research Associate at ICON plc

    Posted: Oct 27, 2026
    Expires: Not specified
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  • We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We are a global provider of consu...

    View All Jobs at ICON plc


     

    Senior Clinical Research Associate

    What You Will Do:

    • You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

    Key responsibilities include:

    • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
    • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
    • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
    • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
    • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

    Your Profile:

    • You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

    Required qualifications and experience:

    • Bachelor's degree in a relevant scientific discipline or healthcare-related field
    • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
    • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
    • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
    • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
    • Willingness to travel as required (approximately 60%)

    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

    Check how your CV matches this job

    Method of Application

    Interested and qualified? Go to ICON plc on icon.wd3.myworkdayjobs.com to apply

    Build your CV for free. Download in different templates.

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