Research Quality Assurance and Compliance Specialist

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. With a reputation for setting the standard of excellence in our field, we continue to transform lives through better vision. 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.Our core values that provide our foundation: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. We use humor as a way to create a less formal, less stressful and more productive work environment.Committed - We are accountable and 100% committed to the Success of VTV. We are boundaryless; we are willing to take initiative to delight our 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!You Are:Ready to live out our core values in patient and team member interactionsDetail-oriented, and a critical thinkerA clear communicator, and able to collaborate with othersAn independent learner who has the ability to problem solveYou Will Make an Impact By:Serving as a subject matter expert on regulatory requirements and clinical trial best practices.Ensuring timely submission of regulatory documents to study sponsors and regulatory agencies.Developing and maintaining internal quality assurance processes to identify and correct potential compliance issues proactively.Serving as a resource during audits and regulatory inspections, and helping facilitate FDA inspections alongside research leaders and study leads.Assisting Vance Thompson Vision sites with submitting study start-up documents to sponsors, and coordinating site activation activities.Designing, developing, and delivering effective training programs for new and existing research team members on topics such as regulatory compliance, documentation, and procedural updates.Establishing and maintaining communication channels to provide critical regulatory updates and changes to research team members.You Have:A Clinical Research Coordinator certificationA minimum of three to five years’ experience in clinical researchPrevious ophthalmology experienceVance Thompson Vision is an equal opportunity and affirmative action employer. We are committed to creating a diverse and inclusive culture for all employees. #J-18808-Ljbffr Vance-Thompson-Vision