Sr. Principal, Medical Science Liaison - Mid Atlantic

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. This role is part of Alcon's Research & Development function, a team that innovates boldly and delivers new products and services to help revolutionize the eye care industry, advance optimal patient outcomes and help people see brilliantly. The ( Science/Tech/Engineering Path) is primarily responsible for presenting scientific and clinical information on Alcon products and gathering insights to influence company strategies. You will drive problem-solving and innovation through scientific principles. In this role, a typical day will include: - Develop andmaintainpeer-to-peer relationships with medical experts and key opinion leaders. - Support the development and adoption of Alcon products through evidence-based scientific exchange and seek external insights. - Provide general medical information in therapeutic areas to practitioners and Alcon associates and respond to unsolicited requests for medical information. - Engage in scientific discussions around Alcon product data. - Implement medical projects and navigate investigator trials frominceptionto publication. - Maintain thorough knowledge of Alcon products and current medical/scientific research. - Work with Med Info and Med Safety to resolve escalated product complaints and medical safetyissues, andparticipate in adverse event reporting and safety responsibilities monitoring. - Direct human clinical trials, phases III and IV for company products under development,monitoradherence to protocols, anddeterminestudy completion. - Provide reporting information for reportssubmittedto regulatory agencies. - Serve as medical consultant to marketing, commercial or research project teams and government regulatory agencies, and act as consultant/liaison with other corporations under licensing agreements. - Sign offonproduct safety reviews. - Interface effectively with all other Medical Affairs functions and departments, including Commercial, Quality Assurance, Research and Development, Regulatory Affairs, Market Access, etc. - Work with integrity and compliance,observinglaws, industry standards, and company policies. - All associates must adhere toGxPregulations by strictly following Standard Operating Procedures (SOPs),maintainingaccurateand complete documentation, ensuring rigorous quality control, and completing all required training. Associatesare responsible formeeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations. WHAT YOU'LL BRING TO ALCON: - Bachelor's Degree or Equivalent years ofdirectly relatedexperience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs). - The ability to fluently read, write,understandand communicate in English. - 7 Years of Relevant Experience. PREFERED EDUCATION AND EXPERIENCE: MD or OD with specialization in Ophthalmology. Advanced knowledge of glaucoma including ophthalmic surgical procedures and optometry. Experience in an ophthalmology or optometry field (academia, industry, clinical practice), including ophthalmic industry or clinical practice. Experience in an ECP-facing role. Working knowledge of the Healthcare System and of the research procedures as well as the ICH guid