Sr. Principal, Medical Science Liaison - Mid Atlantic

11 Locationssenior

OtherMedical Science Liaison

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Requirements Summary

Bachelor’s Degree or Equivalent years of directly related experience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs). The ability to fluently read, write,

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OtherMedical Science Liaison

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 Glaucoma Medical Science Liaison (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 and maintain peer-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 from inception to 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 safety issues, and participate in adverse event reporting and safety responsibilities monitoring.

Direct human clinical trials, phases III and IV for company products under development, monitor adherence to protocols, and determine study completion.

Provide reporting information for reports submitted to 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 off on product 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, observing laws, industry standards, and company policies.

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.

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Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.