Regional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (Southeast & FL [...]
$190.8k - $300.3kMerck
Job Description Regional Medical Scientific Director (RMSD) is a credentialed 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 RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. Role Summary RMSDs liaise 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 RMSD serves as a role model for other field medical team members in ways that include onboarding and/or sharing of therapeutic expertise. Location Location: Southeast (GA, AL, MS, TN) & Florida Panhandle. Candidates must reside within the territory and may travel up to 50% of the time (with some overnight). Responsibilities and Primary Activities Scientific Exchange Develop professional relationships and engage with national and regional SLs to ensure access to company-approved medical and scientific information on therapeutic interests and company products. Conduct peer‑to‑peer scientific discussions and maintain a reliable presence with SLs to ensure they have a medical contact within the company. Address scientific questions and direct SL inquiries on issues outside the RMSD scope to appropriate company resources. Maintain current knowledge of the dynamic scientific and clinical environment in the Company’s Areas of Interest (AOI) for the RMSD’s therapeutic area. Research Upon request from Global Center for Scientific Affairs (GCSA), initiate discussions with SLs and/or potential investigators for scientific/data exchange within our AOI to align with research strategies, study concepts, scientific merit, and qualifications for a specific compound or trial. Enhance comprehension of the scientific foundations and goals of investigator-sponsored research. Identify barriers to patient enrollment and retention efforts to achieve study milestones. Upon request from Global Clinical Trial Operations (GCTO), recommend study sites, identify potential investigators, conduct Site Initiation Visits (SIVs), and detect barriers to patient enrollment and retention to achieve study milestones. Lead protocol responsibilities in collaboration with GCTO. Answer questions from investigators and provide information regarding participation in company-sponsored clinical studies. Scientific Congress Support Engage in scientific congresses and medical meetings, facilitating scientific and data exchange for both company and competitor data. Scientific Insights Gather feedback, data, or information during routine activities that help the company understand medical or scientific needs, priorities, or concerns of SLs and/or patients. Inclusive Mindset and Behavior Demonstrate eagerness to contribute to an environment of belonging, inclusion, equity, and empowerment. Serve as a role model for creating, leading, and retaining a diverse and inclusive workforce. Required Qualifications, Skills, & Experience Minimum PhD, PharmD, OD, DO, or MD. At least 2 years of eye care experience beyond terminal degree program. Ability to conduct doctoral‑level discussions with key external stakeholders. Dedication to scientific excellence with a strong focus on education and dialogue. Excellent stakeholder management, communication, and networking skills. Comprehensive knowledge of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry. 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. Commitment to fostering inclusion, equity, and empowerment through: Engaging to transform culture and business landscape. Leveraging diversity and inclusion to ensure business value per global strategy. Ensuring accountability to drive an inclusive culture. Strengthening foundational elements of diversity. Adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including SOPs, GCP guidelines, and administrative responsibilities. Preferred Retina field‑based medical experience. Salary Range $190,800.00 – $300,300.00 (annual base salary). Eligible for annual bonus and long‑term incentive, if applicable. Benefits Comprehensive package including medical, dental, vision, and other insurance benefits for employee and family; retirement benefits, including 401(k); paid holidays, vacation, compassionate and sick days. Travel Requirements Travel up to 50% of the time within the territory. 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 EEOC Know Your Rights. EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts. Requisition ID
R392173
#J-18808-Ljbffr Merck$190.8k - $300.3k
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