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Job DetailsJob Location: Omaha Clinic – Omaha, NE 68137 Why VTVAt Vance Thompson Vision, we take pride in being global leaders in vision correction, driven by our commitment to groundbreaking research
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Research Quality Assurance and Compliance Supervisor
- Omaha, Nebraska, United States
- Omaha, Nebraska, United States
À propos
Job Location: Omaha Clinic – Omaha, NE 68137 Why VTV
At Vance Thompson Vision, we take pride in being global leaders in vision correction, driven by our commitment to groundbreaking research, innovative technology, and exceptional patient care. We believe that exceptional care begins with an exceptional team. Be part of something greater—join us and discover what it means to create a world‑class culture while making a meaningful impact. Core Values
Caring – We are passionate, empathetic, and sensitive to the needs of our teammates, patients, and everyone we touch. Fun – We choose a positive attitude every day and use humor to create a less formal, less stressful and more productive work environment. Committed – We are accountable and 100% committed to the success of VTV, willing to take initiative to delight customers, motivate fellow teammates and improve financial results. Egalitarian – We play on a team where everyone is equal, where no task is too small for any member to step up and own inside and outside their functional area. Excellence – We are committed to doing the extra work to be outstanding in customer service, patient care and team happiness. Job Opportunity
We are growing and we are looking for a Research and Regulatory Compliance Specialist to join our team. About You
Ready to live out our core values in patient and team member interactions. Detail‑oriented and a critical thinker. A clear communicator, able to collaborate with others. An independent learner who can problem‑solve. Impact
Serve as a subject matter expert on regulatory requirements and clinical trial best practices. Ensure timely submission of regulatory documents to study sponsors and regulatory agencies. Develop and maintain internal quality assurance processes to identify and correct potential compliance issues proactively. Serve as a resource during audits and regulatory inspections, and help facilitate FDA inspections alongside research leaders and study leads. Assist Vance Thompson Vision sites with submitting study start‑up documents to sponsors and coordinating site activation activities. Design, develop, and deliver effective training programs for new and existing research team members on regulatory compliance, documentation, and procedural updates. Establish and maintain communication channels to provide critical regulatory updates and changes to research team members. Qualifications
Clinical Research Coordinator certification. Minimum of three to five years’ experience in clinical research. Previous ophthalmology experience. EEO Statement
Vance Thompson Vision is an equal opportunity and affirmative action employer. We are committed to creating a diverse and inclusive culture for all employees.
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Compétences linguistiques
- English
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