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Clinical Validation Analyst I
Clinical Validation Analyst I-March 2024
Jacksonville
Mar 28, 2026
About Clinical Validation Analyst I

  ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

  Responsibilities:

  • Participate in the execution of the clinical study as delegated by the Principal Investigator

  • Be a team player with the ability to work with a diverse staff in a sponsor environment

  • Ability to multi-task across several projects in a fast paced environment

  • Conduct the Informed Consent process according to FDA regulations and GCP guidelines

  • Accurately record study data into appropriate data collection instrument, e.g. Case Report Form, Electronic Data Capture (EDC)

  • Administer specialized testing to study subjects according to the study protocol

  • Assist Clinical Optometrists as required per protocol to facilitate patient visits and clinic flow

  • Assist with test article dispensing and collection, ensuring proper labeling and storage per Sponsor guidelines

  • Maintain and calibrate specialized optometric equipment as needed

  • Responsible for the safety of clinical subjects and data integrity of clinical trials

  • Obtain essential study documentation and prepare study specific documents (i.e., study enrollment logs, test article dispensing logs, etc.)

  • Verify receipt of test articles, maintain proper storage, and maintain inventory throughout the study

  • Participate in Study Initiation Meetings and coordinate study monitoring visits

  • Assist with subject scheduling and participation in clinical trials

  • Other duties as delegated by management

  Qualifications:

  • High School Diploma

  • Minimum 5 years optometry field experience preferred (i.e., ophthalmic technician, optician, etc.)

  • Certified Para Optometric, Optician license, or other equivalent certification is a plus

  • Clinical research experience is a plus

  • Knowledgeable of relevant FDA regulations and GCP guidelines is a plus

  You are:

  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 maximise savings and plan with confidence for the years ahead

  Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others

  Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

  ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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 (https://careers.iconplc.com/reasonable-accommodations) .

  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.

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