Merck
USMA Regional Medical Scientific Director (RMSD) GI Immunology - Northwest Terri
Merck, Lansing, Michigan, United States, 48900
Overview
The Regional Medical Scientific Director (RMSD) is a credentialed (PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). This MSL-type 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. The RMSD 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 RMSD serves as a role model for other field medical team members in on-boarding and/or sharing therapeutic expertise. This position will support the Company’s Gastrointestinal (GI) Immunology program. Location:
The position covers WA, OR, Northern California and the Northwest.
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 SLs to ensure they have a medical contact within the company Addresses scientific questions and directs SL inquiries on issues outside of RMSD scope (e.g., grants) to appropriate company resources consistent with applicable policies Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the RMSD’s 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 our 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
Clinical Operations Support
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 Protocol lead responsibilities in collaboration with GCTO 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 to help the company better understand medical or scientific needs, priorities, or concerns of SLs and/or patients
Qualifications Required Qualifications, Skills, & Experience PhD, PharmD, DNP, DO, or MD Proven competence and a minimum of 3 years of relevant therapeutic area experience beyond that obtained in 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 Comprehensive understanding 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 Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, SOPs, Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities
Preferred Field-based medical experience Research Experience Demonstrated record of scientific/medical publication
#eligibleforERP
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)
Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
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 diversity and inclusion. Learn more about your rights, including under California, Colorado and other US State Acts.
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be on a Hybrid work model requiring three total days on-site per week, Monday-Thursday, with Friday remote, unless business critical tasks require on-site presence. This does not apply to field-based positions or other specified exemptions.
The salary range for this role is $187,000.00 - $294,400.00. The final salary is based on factors including education, qualifications, experience, skills, location, and business needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive benefits package. More information at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en or via the Workday Jobs Hub if you are a current employee. The application deadline is stated on this posting.
Travel Requirements:
50%
Flexible Work Arrangements:
Remote
VISA Sponsorship:
No
Relocation:
No
Employee Status:
Regular
Hazardous Material(s):
n/a
Required Skills:
Accountability, Clinical Development, Clinical Immunology, Clinical Trials, Data Analysis, Gastroenterology, Good Clinical Practice (GCP), Immunoassays, Immunogenicity Assays, Immunology, Inflammatory Diseases, Leadership, Medical Affairs, Pharmaceutical Medical Affairs, Pharmacy Regulation, Scientific Communications, Site Initiation, Stakeholder Engagement, Stakeholder Management
Travel and other notes:
50% travel; Remote work; Driving license required
This job posting ends on 10/11/2025. A posting is effective until the day before the listed end date.
Requisition ID:
R365786
#J-18808-Ljbffr
The Regional Medical Scientific Director (RMSD) is a credentialed (PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). This MSL-type 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. The RMSD 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 RMSD serves as a role model for other field medical team members in on-boarding and/or sharing therapeutic expertise. This position will support the Company’s Gastrointestinal (GI) Immunology program. Location:
The position covers WA, OR, Northern California and the Northwest.
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 SLs to ensure they have a medical contact within the company Addresses scientific questions and directs SL inquiries on issues outside of RMSD scope (e.g., grants) to appropriate company resources consistent with applicable policies Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the RMSD’s 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 our 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
Clinical Operations Support
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 Protocol lead responsibilities in collaboration with GCTO 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 to help the company better understand medical or scientific needs, priorities, or concerns of SLs and/or patients
Qualifications Required Qualifications, Skills, & Experience PhD, PharmD, DNP, DO, or MD Proven competence and a minimum of 3 years of relevant therapeutic area experience beyond that obtained in 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 Comprehensive understanding 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 Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, SOPs, Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities
Preferred Field-based medical experience Research Experience Demonstrated record of scientific/medical publication
#eligibleforERP
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)
Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
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 diversity and inclusion. Learn more about your rights, including under California, Colorado and other US State Acts.
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be on a Hybrid work model requiring three total days on-site per week, Monday-Thursday, with Friday remote, unless business critical tasks require on-site presence. This does not apply to field-based positions or other specified exemptions.
The salary range for this role is $187,000.00 - $294,400.00. The final salary is based on factors including education, qualifications, experience, skills, location, and business needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive benefits package. More information at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en or via the Workday Jobs Hub if you are a current employee. The application deadline is stated on this posting.
Travel Requirements:
50%
Flexible Work Arrangements:
Remote
VISA Sponsorship:
No
Relocation:
No
Employee Status:
Regular
Hazardous Material(s):
n/a
Required Skills:
Accountability, Clinical Development, Clinical Immunology, Clinical Trials, Data Analysis, Gastroenterology, Good Clinical Practice (GCP), Immunoassays, Immunogenicity Assays, Immunology, Inflammatory Diseases, Leadership, Medical Affairs, Pharmaceutical Medical Affairs, Pharmacy Regulation, Scientific Communications, Site Initiation, Stakeholder Engagement, Stakeholder Management
Travel and other notes:
50% travel; Remote work; Driving license required
This job posting ends on 10/11/2025. A posting is effective until the day before the listed end date.
Requisition ID:
R365786
#J-18808-Ljbffr