Msl - North Central

• Engaging external experts through fair-balanced, evidence-based scientific exchange
• Ensuring compliance with PhRMA Code, internal policies, and all applicable regulations
• Supporting the generation and communication of scientific insights that inform Medical Affairs strategy
• Contributing to pre-launch readiness and pipeline support by building disease state expertise, facilitating clinical trial awareness, and preparing for future product introductions
• 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

• 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)
• Clean and valid driver’s license
• Strong written and oral communication
• Self-Motivation
• Leadership
• Teamwork and Collaboration
• Problem Solving
• Decisiveness
• Time-Management

ophthalmology experience preferred

• Comprehensive medical benefits: we value access to healthcare for our patients as well as our employees
• Generous vacation / holiday time off: we care about our employees and encourage a balanced lifestyle
• Competitive 401(K) matching
• Very generous monthly car allowance