Medical Science Liaison, South/Central USA

🕒 2 days ago

🇺🇸 United States – Remote

💵 $175k - $225k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 0%

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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

• Execute field medical activities supporting Phase 3 clinical trial execution and site engagement within an assigned territory • Develop and maintain scientific relationships with clinical investigators, key opinion leaders, healthcare providers, academic institutions, and other stakeholders • Support investigator and study site engagement, including trial awareness, protocol education, patient identification strategies, and OD referral initiatives • Provide clinical, scientific, and protocol-related support throughout study execution • Partner with Clinical Operations to identify site-level needs, support enrollment objectives, and address scientific or educational barriers • Facilitate compliant scientific exchange regarding clinical data, disease-state education, and clinical development programs • Represent SpyGlass Pharma at scientific congresses, investigator meetings, advisory boards, and clinical insight sessions • Support congress activities, including external engagement, meeting coordination, and collection of field medical insights • Gather, synthesize, and communicate field insights, competitive intelligence, investigator feedback, and unmet medical needs • Collaborate with Clinical Operations, Medical Affairs, Regulatory Affairs, and other cross-functional stakeholders • Contribute to field medical processes, tools, engagement approaches, and best practices • Maintain scientific and clinical knowledge of ophthalmology, glaucoma, ocular hypertension, and related therapeutic areas • Ensure compliance with regulatory requirements, company policies, GCP, and industry standards • Travel extensively within the assigned geography and attend investigator meetings, scientific conferences, and corporate meetings

🎯 Requirements

• Bachelor's degree in life sciences, pharmacy, healthcare, or a related scientific or clinical discipline required • Advanced scientific or clinical degree preferred (PharmD, PhD, OD, MD, NP, PA, or equivalent) • Minimum of 3–5 years of relevant experience within the pharmaceutical, biotechnology, medical device, clinical research, or healthcare industry • Previous MSL, field medical, clinical development, or clinical trial support experience preferred • Experience supporting ophthalmology, glaucoma, ocular hypertension, or related therapeutic areas preferred • Experience supporting late-stage clinical programs or clinical trial site engagement activities preferred • Working knowledge of clinical trial operations, GCP, FDA regulations, and compliant scientific exchange practices • Demonstrated ability to develop effective relationships with investigators, healthcare providers, and other external stakeholders • Strong scientific communication, presentation, and relationship-building skills • Ability to understand and communicate complex scientific and clinical information to diverse audiences • Strong organizational skills with the ability to independently manage multiple priorities and execute responsibilities across an assigned territory • Demonstrated ability to work effectively within cross-functional teams and matrix organizations • Ability to travel up to 50–75% domestically as required • Currently authorized to work in the United States • Comfortable with a travel-based schedule

🏖️ 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

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