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MSD

Regional Medical Scientific Director, MSL, COPD/Respiratory

MSD

. Develop professional relationships and engage with national and regional Scientific Leaders .

Posted 9/22/2026full-timeRemote • United StatesLead💰 $190,800 - $300,300 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in conducting scientific discussions and engaging with key stakeholders in the COPD/Respiratory therapeutic area. Proficient in adhering to regulatory guidelines and facilitating investigator-sponsored research while maintaining strong communication and organizational skills.

Highest-signal resume keywords
PhD, PharmD, DNP, DO, Or MD3 Years Of Relevant Therapeutic Area ExperienceStakeholder ManagementFDA, OIG, HIPAA ComplianceMicrosoft Office Suite

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Scientific DiscussionsClinical Development ProgramsSite Initiation VisitsResearch Alignment AssessmentData Exchange FacilitationPatient Enrollment StrategiesScientific EducationProtocol LeadershipInvestigator EngagementTherapeutic Expertise
Soft Skills
Communication SkillsNetworking SkillsOrganizational SkillsIntegrityEmpowerment
Tools & Technologies
Microsoft Office SuiteVirtual Meeting Platforms
Certifications & Qualifications
PhD, PharmD, DNP, DO, Or MDValid Driving License
Industry Keywords
COPDRespiratoryClinical TrialsGCP GuidelinesEthical GuidelinesInvestigator-Sponsored ResearchScientific LeadersField-Based Medical ExperienceScientific Publication Record

About the role

Key responsibilities & impact
  • Develop professional relationships and engage with national and regional Scientific Leaders
  • Conduct peer-to-peer scientific discussions and provide approved medical and scientific information
  • Address scientific questions and direct out-of-scope inquiries to appropriate company resources
  • Maintain current knowledge of the scientific and clinical environment in COPD/Respiratory
  • Initiate scientific and data exchanges with potential investigators and assess research alignment, study concepts, scientific merit, and qualifications
  • Enhance understanding of investigator-sponsored research foundations and goals
  • Identify barriers to patient enrollment and retention
  • Recommend study sites and identify potential investigators for Phase II-IV clinical development programs
  • Conduct Site Initiation Visits
  • Serve as protocol lead in collaboration with Global Clinical Trial Operations
  • Address investigator questions and provide information about Company-sponsored clinical studies
  • Engage in scientific congresses and medical meetings and facilitate scientific/data exchange
  • Gather scientific insights about medical or scientific needs, priorities, and concerns of Scientific Leaders and/or patients
  • Liaise between the scientific community and the Company
  • Support onboarding and share therapeutic expertise with other field medical team members
  • Adhere to field and corporate policies, GMSA strategy, SOPs, GCP guidelines, and administrative/operational responsibilities
  • Work independently and as a team member while modeling integrity, inclusion, and empowerment

Requirements

What you’ll need
  • Must reside within the Chicago (IL, WI, IA, MN, SD) territory
  • Ability to travel up to 50% within the territory
  • Required credential: PhD, PharmD, DNP, DO, or MD
  • Advanced Practice Providers or MS in a healthcare discipline may be considered with relevant experience
  • Minimum of 3 years of relevant therapeutic area experience beyond that obtained in the terminal degree program, e.g., COPD/Respiratory
  • Excellent stakeholder management, communication, and networking skills
  • 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
  • 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
  • Valid driving license required
  • No visa sponsorship
  • Preferred: field-based medical experience, research experience, and demonstrated scientific/medical publication record

Benefits

Comp & perks
  • Annual bonus
  • Long-term incentive, if applicable
  • Medical, dental, vision healthcare and other insurance benefits for employee and family
  • Retirement benefits, including 401(k)
  • Paid holidays
  • Vacation
  • Compassionate and sick days
  • Remote work arrangement