Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Mid-Atlanti[...]

Job Description We are seeking a Growth and Improvement minded Regional Medical Scientific Director (Medical Science Liaison) in Inflammatory Bowel Disease Immunology that can help drive our Strategic Operating Priorities. Summary, Focus and Purpose The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and 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 is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. You will 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 and serve as a role model for other field medical team members in ways that include onboarding and/or sharing of therapeutic expertise. Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities. 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 areas of therapeutic interest and Company products Conduct peer-to-peer scientific discussions and maintain a reliable presence with those SLs to ensure they have a medical contact within the company Address scientific questions and direct SL inquiries on issues outside of scope (e.g., grants) to appropriate company resources consistent with applicable policies Maintain current knowledge and comprehension of the dynamic scientific and clinical environment in the Company’s Areas of Interest (AOI) for your specific therapeutic area Research Upon request from Global Center for Scientific Affairs (GCSA): initiate discussions with SLs and/or potential investigators to determine alignment with research strategies, study concepts, scientific merit, and qualifications for a specific compound or trial Enhance the 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 and identify potential investigators to participate in phase II–IV clinical development programs, conduct Site Initiation Visits (SIVs), and detect barriers to patient enrollment and retention efforts to achieve study milestones Protocol lead responsibilities in collaboration with GCTO Address questions from investigators and provide information regarding participation in Company-sponsored clinical studies Scientific Congress Support Engage in scientific congresses and medical meetings, facilitate scientific and data exchange for both Company and competitor data Scientific Insights Gather 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 Work independently and as a team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect | Inclusion Demonstrate eagerness to contribute to an environment of belonging, inclusion, equity, and empowerment Lead by example and serve as a role model for creating, leading, and retaining a diverse and inclusive workforce Motivate to contribute to an environment of belonging, engagement, equity, and empowerment Work to transform the environment, culture, and business landscape Leverage diversity and inclusion to ensure business value, per global diversity and inclusion strategy Ensure accountability to drive an inclusive culture Strengthen the foundational elements of diversity Required Location This role covers the Mid-Atlantic region. Candidates must reside within the territory. Ability for travel up to 50% within the territory. Required Education PhD, PharmD, DNP, DO, or MD Required Experience | Skills | Knowledge Proven competence and 3 years of relevant Immunology (Inflammatory Bowel Disease) experience beyond that obtained in the terminal degree program Principled verbal and written communications 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 Preferred Experience | Skills | Knowledge Additional experience in Immunology, Rheumatology, and/or Dermatology Field-based medical experience Research experienced Demonstrated record of scientific/medical publication Required Skills Clinical Trials External Collaboration Immunology Immunotherapy Inflammatory Bowel Diseases Medical Affairs Pharmaceutical Medical Affairs Professional Networking Scientific Communications Strategic Thinking Salary and Benefits The salary range for this role is $190,800.00 - $300,300.00. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at Equal Employment Opportunity 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 U.S. State Acts ( San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance. Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. #J-18808-Ljbffr Merck