Medical Science Liaison (Eastern USA)

Spyglass Pharma

9d•$175,000 - $225,000•Remote

About The Position

SpyGlass Pharma is seeking a Medical Science Liaison (MSL) to join their team. This field-based role will support the company's clinical development programs, with a primary focus on Phase 3 clinical trial execution and site engagement across an assigned territory. The MSL will act as a scientific resource for investigators, healthcare providers, and study site personnel, assisting with protocol education, trial awareness, patient identification, and referral initiatives to ensure effective study execution. The role also involves contributing to broader scientific engagement and the development of SpyGlass Pharma's field medical capabilities as the organization expands. SpyGlass Pharma is focused on improving and preserving the vision of patients with chronic eye diseases through innovative long-term ophthalmic drug delivery technologies. The company has a highly collaborative team with deep expertise in ophthalmology, drug delivery, pharmaceuticals, and medical devices, and is currently advancing its lead program, the SpyGlass BIM-IOL, through Phase 3 clinical development.

Requirements

Bachelor's degree in life sciences, pharmacy, healthcare, or a related scientific or clinical discipline required.
Minimum of 3–5 years of relevant experience within the pharmaceutical, biotechnology, medical device, clinical research, or healthcare industry.
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.
Applicants must be currently authorized to work in the United States and comfortable with a travel-based schedule.

Nice To Haves

Advanced scientific or clinical degree preferred (PharmD, PhD, OD, MD, NP, PA, or equivalent).
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.

Responsibilities

Execute field medical activities supporting Phase 3 clinical trial execution and site engagement within an assigned territory.
Develop and maintain strong scientific relationships with clinical investigators, key opinion leaders (KOLs), healthcare providers (HCPs), academic institutions, and other relevant stakeholders.
Support investigator and study site engagement activities, including trial awareness, protocol education, patient identification strategies, and OD referral initiatives.
Serve as a scientific resource to investigators and site personnel, providing clinical, scientific, and protocol-related support throughout study execution.
Partner closely with Clinical Operations to identify site-level needs, support enrollment objectives, and address scientific or educational barriers impacting study execution.
Facilitate compliant scientific exchange with healthcare professionals regarding clinical data, disease state education, and SpyGlass Pharma's clinical development programs.
Represent SpyGlass Pharma at scientific congresses, investigator meetings, advisory boards, and clinical insight sessions, as appropriate.
Support scientific congress activities, including external engagement, meeting coordination, and collection of relevant field medical insights.
Gather, synthesize, and communicate field insights, competitive intelligence, investigator feedback, and unmet medical needs to appropriate internal cross-functional teams.
Collaborate with Clinical Operations, Medical Affairs, Regulatory Affairs, and other internal stakeholders to ensure alignment of field activities with clinical development priorities.
Contribute to the continued development of field medical processes, tools, engagement approaches, and best practices as organizational needs evolve.
Maintain strong scientific and clinical knowledge of ophthalmology, glaucoma, ocular hypertension, and related therapeutic areas.
Ensure all activities are conducted in compliance with applicable regulatory requirements, company policies, GCP, and industry standards.
Travel extensively within the assigned geography and attend investigator meetings, scientific conferences, and corporate meetings as required.