Clinical Imaging Analyst
- Dublin, Lisbon
- Clinical Data Management
- ICON Full Service & Corporate Support
- Home or Office
Talent Acquisition Business Partner
- Full Service Division
About the role
Clinical Imaging Analyst - Dublin, Ireland
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Clinical Data Analyst to join our dynamic Medical Imaging and Cardiac Safety team at ICON. In this role, you will be instrumental in ensuring data accuracy and quality for independent read analyses, working collaboratively with Imaging Science, Project Management, and Radiology teams. This is an impactful role that supports clinical trial success by refining imaging data quality and advancing the accuracy of imaging-based data analysis. Joining our team means being part of a forward-thinking group dedicated to innovation and excellence in imaging science for clinical research.
What you will be doing:
- Manage and oversee data analysis and quality control for Independent Read data, using Post Read Quality Control (QC) assessments and study-specific criteria checks.
- Input into study risk assessments, proposing tailored risk indicators for central analysis to enhance the holistic Imaging Central Read design.
- Support the setup and testing of data analysis platforms to ensure optimal data processing and integrity.
- Develop and apply Post Read QC parameters to evaluate Independent Read data quality, referencing the Independent Read Charter, Reviewer Training Manual, and EDC System Specification requirements.
- Conduct and supervise Post Read QC and oversight activities within the Imaging team, ensuring compliance with study-specific criteria.
- Review Independent Read data for adherence to study-specific criteria and manage corrections or database changes before external data delivery.
- Independently review clinical study data to identify potential reader performance issues and provide feedback on reader QC failure trends to support any necessary supplemental training.
- Perform quality checks on data exports from Independent Reads as required, ensuring all criteria checks and post-read QC are completed per the Study Specific procedures.
Your profile:
- Associate degree or bachelor’s degree in Radiology
- ARRT (American Registry of Radiologic Technology) Certification
- Experience in imaging and a keen understanding of clinical trials and regulated environments; preferred CRO or Pharma
- Strong organizational skills to manage criteria checks, post-read QC, and documentation within defined study protocols.
- Proficient in Microsoft tools: Excel, Word and Outlook
#LI-MK1#
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.
Visit our careers site to read more about the benefits ICON offers.
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
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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