Clinical Applications Specialist

🕒 June 25

🏄 California – Remote

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💵 $90k - $130k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 18%

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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

• Provide hands-on procedural support during implant cases, offering real-time coaching and troubleshooting to ensure successful use of SpyGlass’s sustained-release drug delivery technology. • Train and coach surgical staff—including surgeons, scrub techs, and circulating nurses—on proper assembly and delivery of the device. • Ensure site teams are confident in integrating SpyGlass’s technology into existing surgical workflows. • Train clinic staff in explaining SpyGlass’s technology and its benefits to patients. • Collaborate with the Clinical Applications Manager and other team members to report procedural feedback and contribute to training improvements. • Maintain compliance with FDA regulations, GCP guidelines, and SpyGlass Pharma’s internal SOPs. • Represent SpyGlass in a professional manner during site visits, meetings, and industry events as needed.

🎯 Requirements

• Bachelor’s degree in life sciences, nursing, healthcare, or a related field preferred • 5+ years of experience in clinical, surgical support, or ophthalmic medical device roles, ideally with cataract surgery • Comfortable providing support and guidance in operating room settings • Demonstrated ability to instruct clinical and surgical staff on device setup and procedural workflow • Strong observational skills and attention to detail during surgical procedures • Clear and professional verbal and written communication skills • Familiarity with clinical research environments and regulatory compliance (e.g., FDA, GCP) • Ability to travel up to 70% to support trial sites across the U.S. • Proficiency in Microsoft Office and clinical documentation systems

🏖️ Benefits

• Comprehensive health, dental, and vision insurance plans • Generous paid time off, including holidays, vacation days, and personal leave • Share in our success with stock options, giving you a stake in the company’s future • Annual Bonus opportunity

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