The Regional Medical Scientific Director is a credentialed (i.e., MD, PhD, or PharmD) therapeutic and disease area expert who engages in both scientific exchange and research support, when requested, with external scientific leaders and investigators in the medical and scientific community. General Medicine RMSDs provide Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to our company related to Neuroscience and Anesthesia and responds to scientific questions from SLs, including questions about our company products and our company data. RMSDs are responsible for facilitating and developing peer-level relationships with scientific leaders in the external medical/scientific community including those investigators who have potential interest in participating in our company research studies. RMSDs provide support for data generation activities including our company sponsored trials and our company Independent Investigator Study Programs as prioritized and requested by our Research & Development Division leadership.
Identify, establish and manage collaborative professional relationships with national, regional and clinical practice scientific leaders (SLs) and investigators to identify and address scientific needs and to ensure access to medical and scientific information on areas of therapeutic interest and our company data or products
Conduct peer-level scientific discussions and maintain a reliable presence to ensure SLs have a our Research & Development Division/ Medical Affairs contact within our company
Engage in proactive non-product discussions regarding scientific issues (e.g., disease states, diagnosis, epidemiology, unmet medical need, and population health, etc) that are intended to enhance scientific discussions or inform/guide our Research & Development Division/GMA and HH strategy or our Research & Development Division research programs
Facilitate appropriate scientific exchange of information with SLs, including integration of scientific knowledge with actionable insights to inform our Research & Development Division and HH strategies
Communicate external stakeholder opinions, insights and feedback on new data, clinical trends and the evolving vaccine landscape to Medical Affairs HQ teams to enhance scientific understanding and inform internal our Research & Development Division strategies
Represent our Research & Development Division at scientific meetings and congresses and contribute to our Research & Development Division debriefs, insight discussions and post-congress reports
Develop and execute territory plans in alignment with global strategy
Support data generation activities when requested by our Research & Development Division leadership, including the our company Investigator Study Program (MISP), by acting as the primary liaison to investigators interested in developing and performing investigator-initiated research
When requested by our Research & Development Division leadership, work to identify potential investigators for consideration of participation in phase II-IV clinical development programs and provide scientific support for our Research & Development Division sponsored trials as needed
Provide in-depth scientific support to Health Systems Teams within USMA
Demonstrate and maintain in-depth knowledge of the assigned disease and therapeutic area(s) through educational efforts, including attendance at relevant conferences, scientific workshops and review of key journals
Fully comply with all company policies and applicable laws, regulations, and ethical standards
Education Minimum Requirement:
Experience- Minimum Requirements:
A minimum of 3 years prior experience in the biotech/pharmaceutical or healthcare environment
A minimum of 3 years of clinical and/or research experience (beyond that obtained in the terminal degree program) in a relevant disease area(s) and demonstrated scientific excellence in the therapeutic area OR 5 yrs. of MSL experience in a relevant TA and demonstration of scientific excellence in the therapeutic area.
Excellent interpersonal, communication, networking and presentation skills" Ability to travel up to 50% of the time overnights and reside in the indicated territory
Deep therapeutic competency; abreast of trends and new information in the therapeutic/translational science area
Ability to network and partner with important external customers, including scientific leaders, investigators, clinical practice leaders and academic affiliated institutions, including treatment guideline members
The ability to consolidate and understand complex data sets, plan and/or execute data analyses, summarize or synthesize data and objectively interpret results
Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, and OIG, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its external stakeholder environment
Must be able to organize, prioritize, and work effectively in a constantly changing environment
Recognition for scientific excellence in the relevant TA as demonstrated by sustained contributions to the TA via strong clinical, academic and/or translational/basic science research experience in the disease area(s) of interest. Experience in both clinical TA practice and owner of independent research and publication in the relevant TA space is highly desirable (i.e., experience in late stage clinical research as an investigator or key study personnel conducting outcomes research, company sponsored trials, or investigator-initiated trials).
5+ years of prior pharmaceutical industry experience (Medical Scientific Liaison or other clinical, medical or research related position) in the relevant TA/disease state
Prior working experience within the given geography and established relationships with relevant therapeutic area stakeholders
Demonstrable effective leadership skills (by example and through accomplishments), and the ability to step forward to handle challenges within scope of authority
Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel)
If you need an accommodation for the application process please email us at email@example.com
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