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Job Description
- Req#: 118910
Ensure the safety and well-being of clinical trial participants
Conduct and oversee clinical trials in accordance with protocol and regulatory requirements
Participate in Site Initiation Meetings and support study start-up activities
Maintain accurate documentation and ensure data integrity
Ensure compliance with protocols; report deviations and adverse events as required
Manage investigational products and coordinate with the IRB
Provide training to clinical staff and delegate responsibilities appropriately
Develop monthly schedules and support daily site operations
Fulfill Principal Investigator (PI) responsibilities for medical device trials
Collaborate on study design, execution, and post-study analysis
Located in or near Johns Creek, GA and available to work Monday–Friday, 10:30 AM – 7:00 PM
Experienced, with at least 3 years of clinical optometry experience
Licensed, holding a current and active Doctor of Optometry license in Georgia
Detail-oriented, with a strong commitment to protocol compliance and patient safety
Collaborative, with excellent communication skills and a team-focused mindset
Organized, able to manage schedules, documentation, and operational tasks efficiently
- 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
Overview
As an Optometrist, you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Responsibilities
What You’ll Be Doing:
Qualifications
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:
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt 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, 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 through the form below.https://careers.iconplc.com/reasonable-accommodationsInterested 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.
About the company
We are a global healthcare intelligence partner with everything you need to take your assets from concept to compound to cure.
Notice
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