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. We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As Sr. Principal Clinical Project Management, you would be responsible for planning, directing, creating, and communicating clinical study time-lines, ensuring consistency of clinical study and processes across clinical trials, overseeing and resolving their operational aspects in line with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection. Prepares clinical development strategy and manages clinical trial budgets, ensuring studies are conducted within clinical trial protocols. This role is on-site in our Fort Worth, Texas location and a typical day would include: • Serve as a senior-level clinical leader, driving innovation, shaping long-term vision, and influencing organizational strategy within clinical project management Provide strategic oversight across the full product lifecycle, from development and testing to launch and post-market monitoring Lead cross-functional collaboration to develop and execute clinical trials with scientific rigor, ensuring adherence to regulatory requirements, Good Clinical Practice (GCP), and standard operating procedures (SOPs) Develop and implement clinical development strategies, guiding study design, trial execution, and risk mitigation Lead the planning, communication, and management of clinical study timelines while supervising operational aspects and resolving complex challenges Maintain up-to-date clinical evaluation reports and lifecycle management documentation, ensuring alignment with business goals Partner with Global Medical Affairs to support long-term strategy, regional and country-level guidance, product claims development, literature reviews, and training Engage in industry thought leadership, representing the organization’s expertise in scientific publications, conferences, and key opinion leader collaborations Support safety management and stakeholder engagement to enhance clinical excellence. All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting 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.