As an Optometrist, you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
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
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:
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