Sr. Principal, Medical Science Liaison - Mid Atlantic
RemoteIllinois, United States or Virginia, United States
Job Summary
Develop and maintain peer-to-peer relationships with medical experts and key opinion leaders to present scientific and clinical information on Alcon products. Support product adoption through evidence-based scientific exchange, gather external insights, and engage in discussions around product data. Implement medical projects and navigate investigator trials from inception to publication, including directing phases III and IV trials, monitoring adherence to protocols, and determining study completion. Resolve escalated product complaints, participate in adverse event reporting, and sign off on product safety reviews. Provide reporting information for regulatory agencies and serve as a medical consultant to marketing, commercial, or research teams. Maintain thorough knowledge of current medical research and adhere strictly to GxP regulations, SOPs, and compliance standards while working 50-60% of the time.
Required Qualifications
- 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, understand and communicate in English
- 7 Years of Relevant 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 guidelines, GCP, and other ethical guidelines
- Essential knowledge of clinical trial design, product development, regulatory requirements, payer landscape, and life cycle management
- Experience in scientific presentations and basic experience in medical writing and biostatistics
- Proven ability and experience developing and fostering peer-to-peer, credible relationships with Medical Experts/decision makers
- Travel Requirements: 50-60%
Desired Qualifications
- 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 guidelines, GCP, and other ethical guidelines
- Essential knowledge of clinical trial design, product development, regulatory requirements, payer landscape, and life cycle management
- Experience in scientific presentations and basic experience in medical writing and biostatistics
- Proven ability and experience developing and fostering peer-to-peer, credible relationships with Medical Experts/decision makers
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