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The Medical Science Liaison (MSL) serves as a scientific and clinical expert within the ophthalmology therapeutic area, responsible for engaging external experts through fair-balanced, evidence-based scientific exchange. This role ensures compliance with PhRMA Code, internal policies, and all applicable regulations while supporting the generation and communication of scientific insights that inform Medical Affairs strategy. The MSL contributes to pre-launch readiness and pipeline support by building disease state expertise, facilitating clinical trial awareness, and preparing for future product introductions. Through congress participation, insight collection, and collaborative teamwork, the MSL advances scientific understanding and strengthens relationships that ultimately support patient care and evidence-based decision-making.
Job Responsibility:
Conducting fair-balanced, evidence-based scientific exchange with ophthalmologists, optometrists and health care professionals
Identifying, profiling, and engaging appropriate external experts based on clinical expertise and scientific relevance
Delivering and discussing approved scientific materials, clinical data, and disease state information in accordance with PhRMA Code and internal policies
Appropriately handling unsolicited off-label questions through approved medical information processes
Accurately and timely entries of interactions and data into compliantly managed CRM systems
Systematically collecting, synthesizing, and reporting ophthalmic clinical and scientific insights from external experts
Ensuring insights are documented accurately and shared through approved systems to inform Medical Affairs strategy
Attending and supporting pre-, during-, and post-congress activities, including scientific exchange, booth coverage, and congress debriefs
Summarizing emerging data and competitive intelligence for internal stakeholders in a compliant manner
Developing disease state expertise and readiness for upcoming product launches
Engaging external experts on pipeline data and evolving treatment paradigms in a compliant, non-promotional manner
Supporting evidence generation activities and clinical trial awareness
Exemplifying a culture of scientific integrity, compliance, and collaboration across the field medical team and organization
Mentoring peers, sharing best practices, and contributing to training materials
Requirements:
Advanced scientific degree (PharmD, PhD, MD, OD, or equivalent) required
Minimum 2–3 years of experience in Medical Affairs or related clinical/scientific role
ophthalmology experience preferred
Strong understanding of clinical research, disease state management, and evidence-based medicine
Excellent communication and presentation skills with the ability to translate complex science into clear, balanced discussions
Demonstrated ability to work independently and manage multiple priorities in a fast-paced environment
Self-motivated, proactive, and able to build strong relationships with internal and external stakeholders
High level of integrity and commitment to compliance with PhRMA Code and company policies
Ability to travel up to 60%, including internationally (including evenings and weekends for congresses and meetings)