Senior Principal, Medical Science Liaison

🔥 14 minutes ago

⚜️ Louisiana, Mississippi, +1 more states – Remote

⚜️ Louisiana – Remote 🎸 Mississippi – Remote 🌴 South Carolina – Remote

⏰ Full Time

🟠 Senior

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Alcon

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

Alcon is a leading company in the field of eye care, committed to innovating life-changing vision products. Their mission is to help people see brilliantly, enhancing their quality of life. Alcon recently introduced the PRECISION7® contact lens, a revolutionary one-week replacement lens designed to provide clear vision and comfort. With a strong emphasis on research and development, Alcon is dedicated to advancing eye health globally.

📋 Description

• Develop and maintain peer-to-peer relationships with medical experts and key opinion leaders • Support development and adoption of Alcon products through evidence-based scientific exchange and gather external insights • Provide general medical information to practitioners and Alcon associates and respond to unsolicited medical information requests • Engage in scientific discussions about 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 Medical Information and Medical Safety to resolve escalated product complaints and medical safety issues • Participate in adverse event reporting and safety-responsibility monitoring • Direct Phase III and IV human clinical trials, monitor protocol adherence, and determine study completion • Provide reporting information for submissions to regulatory agencies • Serve as medical consultant to marketing, commercial, research, and regulatory teams and licensing-agreement corporations • Sign off on product safety reviews • Interface with Medical Affairs and Commercial, Quality Assurance, Research and Development, Regulatory Affairs, and Market Access departments • Follow laws, industry standards, company policies, GxP regulations, SOPs, documentation, quality control, and required training

🎯 Requirements

• Bachelor’s Degree or equivalent years of directly related experience • Alternative experience equivalencies: high school + 15 years; Associate degree + 11 years; M.S. + 4 years; PhD + 3 years • Fluent ability to read, write, understand and communicate in English • 7 years of relevant experience • Advanced knowledge of glaucoma, including ophthalmic surgical procedures and optometry • Experience in an ophthalmology or optometry field, including ophthalmic industry or clinical practice • Experience in an ECP-facing role • Working knowledge of the healthcare system, research procedures, ICH guidelines, GCP, and other ethical guidelines • Knowledge of clinical trial design, product development, regulatory requirements, payer landscape, and life cycle management • Experience in scientific presentations, medical writing, and biostatistics • Proven ability and experience developing and fostering peer-to-peer relationships with medical experts and decision makers • Ability to comply with GxP regulations, SOPs, documentation, quality control, training, laws, industry standards, and company policies • MD or OD with specialization in Ophthalmology (preferred)

🏖️ Benefits

• Health benefits • Life benefits • Retirement benefits • Flexible time off