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Vice President, Medical Affairs

🕒 September 9

🏄 California – Remote

infoinfo

💵 $325k - $385k / year

⏰ Full Time

🔴 Lead

👔 Vice President

Apply Now
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Logo of SpyGlass Pharma, Inc.

SpyGlass Pharma, Inc.

11 - 50 employees

Founded 2019

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 $75M Series D - Spyglass Pharma on 2025-06

Healthcare • Manufacturing • Biotechnology

<SpyGlass Pharma, Inc. > SpyGlass Pharma, Inc. is a clinical-stage company developing the BIM-IOL System, a sustained drug-delivery intraocular lens designed to deliver long-acting glaucoma therapy at the time of cataract surgery. The technology integrates glaucoma treatment with a trusted surgical procedure to address gaps in adherence and chronic disease management, and the company is advancing the device through preclinical studies and clinical trials (first-in-human, Phase 1/2, and Phase 3).

📋 Description

• Develop and lead the overall Medical Affairs strategy supporting late-stage clinical development, launch readiness, commercialization, and lifecycle management • Build, scale, and lead the Medical Affairs organization, including field medical and medical education capabilities • Establish objectives, processes, infrastructure, and performance expectations • Maintain an active field presence and oversee Medical Affairs activities supporting clinical trial execution • Lead investigator and site engagement, scientific exchange, and trial awareness in collaboration with Clinical Development and Clinical Operations • Lead Medical Affairs launch readiness and execution, including medical education, scientific communications, congress strategy, KOL engagement, and evidence generation • Develop and maintain strategic scientific relationships with KOLs, investigators, treatment centers, academic institutions, and external healthcare stakeholders • Lead scientific advisory boards, steering committees, investigator meetings, and other external scientific engagements • Serve as a senior medical and scientific representative for SpyGlass Pharma • Lead CME, grants, sponsorships, speaker programs, peer-to-peer education, and scientific and clinical training for field-based teams • Lead evidence generation strategy, including real-world evidence programs, post-marketing studies, investigator-initiated research, and related initiatives • Oversee scientific communications and publications, including congress abstracts, presentations, manuscripts, and other scientific content • Partner with Market Access on HEOR, value dossiers, and scientific exchange with payer and healthcare stakeholders • Lead Medical Affairs participation in medical and promotional review processes and provide medical support for regulatory interactions and product labeling activities • Ensure compliance with regulatory requirements, industry standards, company policies, and scientific exchange and medical education requirements • Partner with Commercial leadership to align medical and commercial strategies while maintaining scientific integrity and compliance • Collaborate with Clinical Development on lifecycle management, indication expansion, evidence-generation priorities, and clinical trial planning • Partner with Quality, Safety, Regulatory Affairs, and other stakeholders on post-market medical monitoring and pharmacovigilance • Gather and communicate medical insights, scientific trends, competitive intelligence, and unmet medical needs • Develop and manage Medical Affairs budgets, resource planning, and external partnerships

🎯 Requirements

• Advanced scientific or clinical degree required (MD, PhD, PharmD, OD, or equivalent) • Minimum of 15 years of progressive Medical Affairs experience within the pharmaceutical or biotechnology industry, including significant leadership experience • Demonstrated experience leading Medical Affairs organizations through late-stage clinical development, pre-launch, launch, and post-launch activities • Prior ophthalmology Medical Affairs and product launch experience strongly preferred • Experience with sustained drug delivery, drug-device combination products, or related technologies preferred • Demonstrated experience building, scaling, and leading field medical and Medical Affairs organizations • Strong understanding of late-stage clinical development, clinical trial support, launch readiness, evidence generation, medical education, scientific communications, and lifecycle management • Demonstrated success developing and maintaining strategic relationships with KOLs, investigators, academic institutions, and other external scientific stakeholders • Experience developing and executing medical education, publication, evidence-generation, and scientific engagement strategies • Strong understanding of applicable FDA regulations, industry standards, compliant scientific exchange, medical education, and promotional review requirements • Excellent scientific communication and presentation skills, with the ability to translate complex clinical and scientific information for diverse audiences • Ability to travel domestically up to 50% • Ability to travel internationally, as business needs require

🏖️ Benefits

• Annual Bonus opportunity • Stock options • Comprehensive health, dental, and vision insurance plans • Generous paid time off, including holidays, vacation days, and personal leave • Reasonable accommodation for individuals with disabilities

Apply Now

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