Regional Director, Medical Science Liaison (Eastern USA)

Spyglass Pharma

$225K — $250K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Advanced scientific or clinical degree preferred (PharmD, PhD, OD, MD, NP, or PA).
  • Minimum of 8 years in pharmaceutical, biotechnology, or medical device industries, with field medical affairs or MSL leadership experience.
  • Experience in ophthalmology, glaucoma, retinal care, or related therapeutic areas strongly preferred.
  • Proven experience with Phase 3 clinical programs and investigator engagement activities.
  • Strong understanding of clinical trial operations, GCP, FDA regulations, and compliant scientific exchange.
  • Demonstrated ability in engaging healthcare providers and key opinion leaders.

Responsibilities

  • Lead medical affairs activities for Phase 3 clinical trial execution.
  • Develop scientific relationships with KOLs, healthcare providers, and academic institutions.
  • Support investigator engagement, trial awareness, and patient identification strategies.
  • Serve as a scientific resource throughout study execution for investigators.
  • Establish scalable medical organization and lead regional Medical Science Liaison team.
  • Drive targeted engagement with healthcare systems and strategic accounts.
  • Support strategic objectives and quarterly engagement across top accounts.

Benefits

  • Stock options to share in company success.
  • Comprehensive health, dental, and vision insurance for you and your family.
  • Generous paid time off including holidays, vacation days, and personal leave.
Full Job Description
Summary:

We are seeking a Regional Director, Medical Science Liaison (MSL) to join our team at SpyGlass Pharma. The Regional Director, MSL is responsible for leading scientific engagement and medical affairs activities across a defined territory in support of SpyGlass Pharma's clinical development and commercialization objectives. This position serves as a key scientific resource to healthcare providers, investigators, and strategic healthcare organizations, supporting Phase 3 clinical trial execution, investigator engagement, protocol education, and disease state awareness initiatives. The Regional Director will collaborate closely with Clinical Operations, Medical Affairs, Commercial, and Regulatory teams to support external scientific exchange, congress activities, advisory boards, and key account engagement initiatives focused on ophthalmology and glaucoma care.

Essential Duties & Responsibilities:

  • Lead regional medical affairs activities supporting Phase 3 clinical trial execution.
  • Develop and maintain scientific relationships with investigators, key opinion leaders (KOLs), healthcare providers (HCPs), academic institutions, and integrated delivery networks.
  • Support investigator and 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 by providing clinical and protocol-related support throughout study execution.
  • Establish the foundation for a scalable field medical organization, with responsibility for future team expansion, organizational design, and leadership of Medical Science Liaison professionals across multiple geographic regions.
  • Drive engagement with targeted healthcare systems, physician enterprise groups, HMOs, academic institutions, and strategic ophthalmology accounts.
  • Support development and execution of quarterly engagement objectives across top target accounts and strategic customer groups.
  • Represent SpyGlass Pharma at scientific congresses, advisory boards, investigator meetings, and clinical insight sessions.
  • Support congress planning activities, including scientific exchange planning, meeting coordination, and field medical insights collection.
  • Facilitate compliant scientific exchange with healthcare professionals regarding clinical data, disease state education, and pipeline development activities.
  • Partner with Commercial and Medical Affairs leadership to support speaker bureau identification, onboarding, and training initiatives.
  • Gather and communicate field insights, competitive intelligence, and unmet medical needs to internal cross-functional teams.
  • Collaborate closely with Clinical Operations, Regulatory Affairs, and Commercial teams to ensure alignment of medical strategies and field activities.
  • Maintain deep 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, and industry standards.
  • Ability to travel extensively within assigned geography and attend national conferences, investigator meetings, and corporate meetings as required.


Qualifications Required For Position:

  • Advanced scientific or clinical degree preferred (PharmD, PhD, OD, MD, NP, or PA).
  • Minimum of 8 years of experience within the pharmaceutical, biotechnology, or medical device industry, including field medical affairs or MSL leadership experience.
  • Experience supporting ophthalmology, retina, glaucoma, ocular hypertension, or related therapeutic areas strongly preferred.
  • Experience supporting Phase 3 clinical programs, investigator-sponsored research, or clinical trial site engagement activities preferred.
  • Strong understanding of clinical trial operations, GCP, FDA regulations, and compliant scientific exchange practices.
  • Demonstrated experience engaging with healthcare providers, academic institutions, integrated delivery networks, and key opinion leaders.
  • Excellent scientific communication, presentation, and relationship-building skills.
  • Ability to analyze and communicate complex scientific and clinical information to diverse audiences.
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
  • Demonstrated ability to work effectively within cross-functional teams and matrix organizations.


Please note: This is a U.S. based, remote position that requires regular travel across the country (50-75% domestically as required.). Applicants must be currently authorized to work in the United States and comfortable with a travel-based schedule.

  • We are offering a range of $225,000 - $250,000, based on experience and qualifications, along with an Annual Bonus opportunity.
  • Share in our success with stock options, giving you a stake in the company's 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.

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