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Senior Principal, Medical Science Liaison – VitRet

🕒 September 17

🌽 Illinois, New York, +2 more states – Remote

infoinfo

💵 $152.2k - $196.9k / year

⏰ Full Time

🟠 Senior

Where this job comes from

Posted on Alcon's careers page, not through a job board

First seen by Remote Rocketship September 17

Still open on Alcon's site. Checked 6 hours ago.

Logo of Alcon

Alcon

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

• Present scientific and clinical information on Alcon products • Gather external insights to influence company strategies • 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 • Provide general medical information to practitioners and Alcon associates • Respond to unsolicited requests for medical information • 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 Med Info and Med 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 regulatory agency submissions • Serve as medical consultant to marketing, commercial, research, and regulatory teams • Act as consultant/liaison with corporations under licensing agreements • Sign off on product safety reviews • Interface with Medical Affairs and departments including Commercial, Quality Assurance, Research and Development, Regulatory Affairs, and Market Access • Follow GxP regulations, SOPs, documentation, quality control, and required training requirements

🎯 Requirements

• Bachelor’s Degree or equivalent years of directly related experience • Alternative qualification: high school plus 15 years of directly related experience • Alternative qualification: associate degree plus 11 years of directly related experience • Alternative qualification: M.S. plus 4 years of directly related experience • Alternative qualification: PhD plus 3 years of directly related experience • 7 years of relevant experience • Fluency in reading, writing, understanding, and communicating in English • Ability to travel 75% • Knowledge of GxP regulations and Standard Operating Procedures (SOPs) • Compliance with applicable laws, industry standards, company policies, and regulatory requirements

🏖️ Benefits

• Focused growth and development opportunities • Health benefits • Life insurance • Retirement benefits • Flexible time off • Programs supporting health and well-being • Financial security programs • Retirement planning support • Short-term incentive opportunities for eligible roles • Long-term incentive opportunities for eligible roles • Reasonable accommodation for individuals with disabilities

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