Regional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (
Merck, Helena, Montana, us, 59604
Job Description
Position Title: Regional Medical Scientific Director (RMSD)
Role Summary
The RMSD is a credentialed (PhD, PharmD, OD, DO, or MD) therapeutic and disease expert who engages in bidirectional scientific exchange with Scientific Leaders (SLs), provides balanced, factual information about non‑product interests, and replies to scientific questions from SLs, including those about Company products. Their work aligns with Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.
They liaise between the scientific community and the Company to enhance understanding of scientific foundations and goals for approved, in‑development, and active Company‑sponsored trials, as well as investigator‑sponsored research. They model best practices for onboarding and sharing therapeutic expertise with other field medical team members.
Location Details This role covers Florida & Georgia. Candidates must reside within the territory and be prepared to travel up to 50% of the time (occasionally overnight) within the territory.
Responsibilities and Primary Activities Scientific Exchange
Develop and maintain professional relationships 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 serve as a medical contact within the company.
Address scientific questions and direct SL inquiries on issues outside the RMSD scope (e.g., grant matters) to appropriate company resources in accordance with applicable policies.
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 to exchange scientific/data information within our AOI, evaluating alignment with research strategies, study concepts, scientific merit, and qualifications for specific compounds or trials.
Enhance the comprehension of the scientific foundations and goals of investigator‑sponsored research.
Identify barriers to patient enrollment and retention to achieve study milestones.
Upon request from Global Clinical Trial Operations (GCTO), recommend study sites and identify potential investigators for phase II‑IV clinical development programs; conduct Site Initiation Visits (SIVs); detect barriers to enrollment and retention.
Assume 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, facilitating scientific and data exchange for both the Company and its competitors.
Scientific Insights
Gather feedback, data, or information during routine activities that help the Company better understand medical or scientific needs, priorities, or concerns of SLs and/or patients.
Inclusive Mindset and Behavior
Demonstrate eagerness to contribute to an inclusive environment of belonging, equity, and empowerment.
Lead by example and 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
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
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 an inclusive culture, including transforming the workplace, leveraging diversity, ensuring accountability, and strengthening foundational elements of diversity
Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including SOPs, Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities
Preferred
Retina field‑based medical experience
U.S. Hybrid Work Model Effective September 5, 2023, employees in office‑based positions in the U.S. will work a hybrid schedule of three on‑site days per week (M‑T‑W), with Friday remote. This model does not apply to field‑based roles or positions requiring full on‑site presence.
Salary and Benefits Salary Range: $190,800.00 – $300,300.00 (based on education, qualifications, experience, location, and business needs). Eligible for annual bonus and long‑term incentive, if applicable.
Benefits include medical, dental, vision, retirement (401(k)), paid holidays, vacation, and compassionate and sick days. More information:
Benefits Overview .
Application Information Apply at
https://jobs.merck.com/us/en
(or via the Workday Jobs Hub for current employees). Deadline is indicated on the posting.
Equal Employment Opportunity Statement As an Equal Employment Opportunity Employer, we provide equal opportunities for all employees and applicants 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. We comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under U.S. EEO laws, visit
EEOC Know Your Rights . EEOC GINA Supplement. We celebrate diversity and encourage respectful collaboration.
#J-18808-Ljbffr
Role Summary
The RMSD is a credentialed (PhD, PharmD, OD, DO, or MD) therapeutic and disease expert who engages in bidirectional scientific exchange with Scientific Leaders (SLs), provides balanced, factual information about non‑product interests, and replies to scientific questions from SLs, including those about Company products. Their work aligns with Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.
They liaise between the scientific community and the Company to enhance understanding of scientific foundations and goals for approved, in‑development, and active Company‑sponsored trials, as well as investigator‑sponsored research. They model best practices for onboarding and sharing therapeutic expertise with other field medical team members.
Location Details This role covers Florida & Georgia. Candidates must reside within the territory and be prepared to travel up to 50% of the time (occasionally overnight) within the territory.
Responsibilities and Primary Activities Scientific Exchange
Develop and maintain professional relationships 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 serve as a medical contact within the company.
Address scientific questions and direct SL inquiries on issues outside the RMSD scope (e.g., grant matters) to appropriate company resources in accordance with applicable policies.
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 to exchange scientific/data information within our AOI, evaluating alignment with research strategies, study concepts, scientific merit, and qualifications for specific compounds or trials.
Enhance the comprehension of the scientific foundations and goals of investigator‑sponsored research.
Identify barriers to patient enrollment and retention to achieve study milestones.
Upon request from Global Clinical Trial Operations (GCTO), recommend study sites and identify potential investigators for phase II‑IV clinical development programs; conduct Site Initiation Visits (SIVs); detect barriers to enrollment and retention.
Assume 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, facilitating scientific and data exchange for both the Company and its competitors.
Scientific Insights
Gather feedback, data, or information during routine activities that help the Company better understand medical or scientific needs, priorities, or concerns of SLs and/or patients.
Inclusive Mindset and Behavior
Demonstrate eagerness to contribute to an inclusive environment of belonging, equity, and empowerment.
Lead by example and 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
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
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 an inclusive culture, including transforming the workplace, leveraging diversity, ensuring accountability, and strengthening foundational elements of diversity
Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including SOPs, Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities
Preferred
Retina field‑based medical experience
U.S. Hybrid Work Model Effective September 5, 2023, employees in office‑based positions in the U.S. will work a hybrid schedule of three on‑site days per week (M‑T‑W), with Friday remote. This model does not apply to field‑based roles or positions requiring full on‑site presence.
Salary and Benefits Salary Range: $190,800.00 – $300,300.00 (based on education, qualifications, experience, location, and business needs). Eligible for annual bonus and long‑term incentive, if applicable.
Benefits include medical, dental, vision, retirement (401(k)), paid holidays, vacation, and compassionate and sick days. More information:
Benefits Overview .
Application Information Apply at
https://jobs.merck.com/us/en
(or via the Workday Jobs Hub for current employees). Deadline is indicated on the posting.
Equal Employment Opportunity Statement As an Equal Employment Opportunity Employer, we provide equal opportunities for all employees and applicants 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. We comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under U.S. EEO laws, visit
EEOC Know Your Rights . EEOC GINA Supplement. We celebrate diversity and encourage respectful collaboration.
#J-18808-Ljbffr