
Medical Science Liaison, South/Central USA
Posted Aug 21

Posted Aug 21
This is a fully remote position, open to applicants in United States.
• Implement field medical initiatives to support Phase 3 clinical trial execution and site engagement within a designated region.
• Establish and nurture scientific relationships with clinical investigators, key opinion leaders, healthcare professionals, academic institutions, and other relevant stakeholders.
• Assist in engaging investigators and study sites, encompassing trial awareness, protocol education, patient identification strategies, and OD referral initiatives.
• Provide clinical, scientific, and protocol-related assistance throughout the study execution process.
• Collaborate with Clinical Operations to assess site-level needs, support enrollment objectives, and tackle scientific or educational challenges.
• Facilitate compliant scientific discussions regarding clinical data, disease-state education, and clinical development programs.
• Represent SpyGlass Pharma at scientific congresses, investigator meetings, advisory boards, and clinical insight sessions.
• Assist with congress activities, including external engagement, meeting organization, and gathering field medical insights.
• Collect, analyze, and convey field insights, competitive intelligence, investigator feedback, and unmet medical needs.
• Work in partnership with Clinical Operations, Medical Affairs, Regulatory Affairs, and other cross-functional partners.
• Contribute to the development of field medical processes, tools, engagement strategies, and best practices.
• Maintain a strong scientific and clinical understanding of ophthalmology, glaucoma, ocular hypertension, and associated therapeutic areas.
• Ensure adherence to regulatory requirements, company policies, GCP, and industry standards.
• Travel extensively within the designated geography and participate in investigator meetings, scientific conferences, and corporate gatherings.
• A bachelor's degree in life sciences, pharmacy, healthcare, or a related scientific or clinical discipline is required.
• An advanced scientific or clinical degree is preferred (PharmD, PhD, OD, MD, NP, PA, or equivalent).
• At least 3–5 years of relevant experience in the pharmaceutical, biotechnology, medical device, clinical research, or healthcare sectors.
• Previous experience as an MSL, in field medical roles, clinical development, or clinical trial support is preferred.
• Experience in ophthalmology, glaucoma, ocular hypertension, or related therapeutic fields is preferred.
• Familiarity with late-stage clinical programs or clinical trial site engagement activities is preferred.
• Knowledge of clinical trial operations, GCP, FDA regulations, and compliant scientific exchange practices is essential.
• Proven ability to cultivate effective relationships with investigators, healthcare providers, and other external stakeholders.
• Strong skills in scientific communication, presentation, and relationship-building.
• Capability to comprehend and convey complex scientific and clinical information to varied audiences.
• Excellent organizational skills with the ability to independently manage multiple priorities and responsibilities across a designated territory.
• Demonstrated effectiveness in working within cross-functional teams and matrix organizations.
• Willingness to travel up to 50–75% domestically as needed.
• Must be currently authorized to work in the United States.
• Comfortable with a travel-intensive schedule.
• Opportunity for an annual bonus.
• Stock options available.
• Comprehensive health, dental, and vision insurance coverage.
• Generous paid time off, including holidays, vacation days, and personal leave.
• Reasonable accommodations for individuals with disabilities.
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