R&D Program Manager

About SpyGlass Pharma:

At SpyGlass Pharma (NASDAQ: SGP) we are focused on improving and preserving the vision of patients living with chronic eye diseases while minimizing the burden treatment can place on their daily lives. We are advancing innovative long-term ophthalmic drug delivery technologies designed to provide sustained therapy through cataract surgery and help improve patient outcomes.

We have built a highly collaborative team with deep expertise across ophthalmology drug delivery pharmaceuticals and medical devices. Our scientists engineers and clinical leaders bring decades of experience developing and commercializing breakthrough technologies united by a shared commitment to patients and our guiding principle: We create for patients. That mindset shapes how we build our products our teams and our culture.

Backed by strong clinical progress significant funding and a growing organization SpyGlass Pharma is entering an exciting stage of growth as we advance our lead program the SpyGlass BIM-IOL through Phase 3 clinical development.

Summary:

SpyGlass Pharma is seeking a high-potential R&D Program Manager with strong execution focus to join our growing Program Management team. Reporting to the Senior Director of Program Management this role will support and gradually take on leadership of cross-functional R&D projects across the product development lifecycle ensuring alignment of activities timelines and deliverables.

This position is ideal for candidates with hands-on experience in pharmaceutical or medical device R&D who are looking to expand into program management and build capabilities in integrated planning cross-functional coordination and program execution.

The successful candidate will bring strong operational discipline attention to detail and the ability to connect interdependent activities to drive project outcomes in a fast-paced high-growth environment while gaining exposure to broader program objectives and company priorities. This role offers the opportunity to progressively take on increased ownership and responsibility with a clear path toward leading cross-functional programs.

Essential Duties & Responsibilities:

• Supports development and maintenance of cross-functional project plans including timelines milestones and dependencies
• Tracks progress against deliverables and proactively identifies risks delays and downstream impacts across functions
• Contributes to ensuring functional activities are aligned into a cohesive executable project plan
• Coordinates with Clinical Regulatory CMC and other functions to ensure alignment on timelines deliverables and priorities
• Drives follow-up on action items and ensures accountability across team members
• Builds strong working relationships across functions to support effective collaboration
• Identifies assesses and tracks project risks and issues including potential impact on timelines scope and key milestones
• Escalates risks and issues in a timely manner providing clear context and potential impact to support decision-making
• Prepares project status updates dashboards and presentations for team and leadership review
• Facilitates team meetings including agenda development clear documentation of decisions and tracking of action items to closure
• Maintains organized and accurate project documentation and repositories ensuring accessibility and consistency across timelines presentations and team materials
• Contributes to business process and systems improvement through Program Management departmental assignments
  

Qualifications Required For Position:

• Bachelors degree in science engineering or related discipline
• 36 years of experience in pharmaceutical biotechnology or medical device R&D including experience supporting cross-functional projects or project management activities
• Foundational understanding of product development lifecycles (early stage through clinical to commercialization) and regulatory environment governing drug and device development
• Demonstrated ability to manage multiple priorities and identify dependencies across workstreams in a cross-functional environment
• Strong organizational analytical and problem-solving skills
• Excellent written and verbal communication skills

Qualifications Preferred For Position:

• Project Management Professional (PMP) certification or training
• Experience within one or more R&D functions (e.g. Clinical CMC Product Development) in pharmaceutical biotechnology or medical device environments
• Experience supporting cross-functional projects or development programs
• Familiarity with project management tools (e.g. MS Project Smartsheet or similar platforms)
• Experience in ophthalmology or combination product development (strong plus)

Why SpyGlass Pharma

• We are offering a range of $140000 - $160000 based on experience and qualifications along with an Annual Bonus opportunity.
• Share in our success with stock options giving you a stake in the companys future.
• Comprehensive health dental and vision insurance plans to keep you and your family healthy and happy with a variety of plan and coverage options.
• Generous paid time off including holidays vacation days and personal leave.

SpyGlass Pharma is an Equal Opportunity Employer and participates in E-Verify. SpyGlass Pharma takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment hiring training promotion or other employment practices for reasons of race color religion gender national origin age sexual orientation gender identity marital or veteran status disability or any other legally protected status.

SpyGlass Pharma is also committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position please send an email to and let us know the nature of your request and your contact information.

Required Experience:

Manager