Regional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (Nor CA)

Role Summary The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. The Regional Medical Scientific Director liaises between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in‑development, and active Company-sponsored trials and/or investigator-sponsored research studies. The Regional Medical Scientific Director serves as a role model for other field medical team members in ways that include on‑boarding and/or sharing of therapeutic expertise. Location This role covers Northern California. Candidates must reside within the territory and can travel up to 50% (with some overnight) within the territory. Responsibilities and Primary Activities Scientific Exchange Develops professional relationships and engages with national and regional SLs to ensure access to company-approved medical and scientific information on areas of therapeutic interest and Company products. Conducts peer‑to‑peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company. Addresses scientific questions and directs SL inquiries on issues outside of Regional Medical Scientific Director scope (e.g., grants) to appropriate company resources consistent with applicable policies. Maintains current knowledge and comprehension of the dynamic scientific and clinical environment in the Company's Areas of Interest for the specific therapeutic area. Research Upon request from Global Center for Scientific Affairs (GCSA), initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine alignment with research strategies, study concepts, scientific merit, and qualifications for a specific compound or trial. Enhances the comprehension of the scientific foundations and goals of investigator‑sponsored research. Identifies barriers to patient enrollment and retention efforts to achieve study milestones. Protocol Lead Responsibilities Upon request from Global Clinical Trial Operations (GCTO), recommends study sites and identifies potential investigators to participate in phase II–IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention to achieve study milestones. Addresses questions from investigators and provides information regarding participation in Company‑sponsored clinical studies. Scientific Congress Support Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both Company and competitor data. Scientific Insights Gathers feedback, data, or information during routine activities that can help the company better comprehend medical or scientific needs, priorities, or concerns of SLs and/or patients. Inclusive Mindset and Behavior Demonstrates eagerness to contribute to an environment of belonging, inclusion and empowerment. Leads by example and serves as a role model for creating, leading, and retaining a workforce. Qualifications and Experience Minimum PhD, PharmD, OD, DO, or MD Proven competence and a minimum of 2 years of Eye Care experience beyond the terminal degree program Ability to conduct doctoral‑level discussions with key external stakeholders Dedication to scientific excellence with a strong focus on scientific education and dialogue Excellent stakeholder management, communication, and networking skills Thorough comprehension of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers Ability to organize, prioritize, and work effectively in a constantly changing environment Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Teams, OneNote) Familiarity with virtual meeting platforms Desire to contribute to an environment of belonging, engagement, and empowerment Strong adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field SOPs, Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities Preferred: Retina field‑based medical experience Benefits Salary range: $190,800.00 – $300,300.00 (and additional considerations based on qualifications) Eligible for annual bonus and long‑term incentive, if applicable Comprehensive package of benefits, including medical, dental, vision, retirement benefits (401(k)), paid holidays, vacation, and compassionate and sick days Equal Employment Opportunity Statement As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit the EEOC Know Your Rights page. We are proud to be a company that embraces diversity and inclusion. #J-18808-Ljbffr MSD Malaysia