.Johnson & Johnson is currently seeking a Staff Clinical Research Scientist to join the Surgical Vision team located in Irvine, CA, Milpitas, CA, or Jacksonville, FL.At Johnson & Johnson, we believe health is everything.Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges. We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities, and experiences are valued and our people can reach their potential.As a Clinical Scientist in the Surgical Vision platform, you will be part of a high-functioning team with core expertise in ophthalmology and medical device research. You'll be an integral part of your cross-functional project teams, devising clinical strategy and delivering results that help create new products that drive the business.Key Responsibilities Represent Clinical Science in cross-functional project team meetings, provide project team requirements as needed, with input/guidance from senior function members.Align with Clinical Operations team (study managers, CRAs) on project status/updates and identify issues or impact to project timelines as appropriate.Plan, design and develop/write documents required for clinical projects, including protocol outlines, protocol procedures, and reports.Draft, revise and perfect written materials in alignment with colleagues and partners to produce landmark scientific publications, including conference posters, KOL presentations, and technical or promotional documents.Operate in accordance with functional and enterprise SOPs, ensure training is complete and current.Evaluate and interpret clinical research data to ensure timely and accurate data analysis to be presented in a way that fairly and accurately reflects study results.Qualifications Education:· Bachelor's degree in a scientific field is required, advanced degree is preferred (Doctorate in Optometry or MD or Ph.D. or equivalent)