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MSD

Regional Medical Scientific Director – Gynecologic Malignancies

MSD

. Engage in bidirectional scientific and medical information exchange with Scientific Leaders .

Posted 10/8/2026full-timeRemote • United StatesLead💰 $210,400 - $331,100 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in scientific communication and stakeholder engagement, with a strong focus on ethical guidelines and regulatory compliance in the pharmaceutical industry. Proven ability to conduct high-level discussions and support clinical development through strategic relationships with Scientific Leaders and investigators.

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

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 CommunicationClinical DevelopmentResearch StrategiesStudy Site RecommendationsProtocol Leadership SupportInvestigator EngagementScientific PublicationPatient Enrollment StrategiesData Exchange FacilitationTherapeutic Area Knowledge
Soft Skills
Networking SkillsOrganizational SkillsPrioritization SkillsAdaptabilityDedication To Scientific Excellence
Tools & Technologies
Microsoft Office SuiteVirtual Meeting Platforms
Industry Keywords
GYN OncologyClinical ResearchEthical GuidelinesGCP GuidelinesField SOPsGMSA Strategy

About the role

Key responsibilities & impact
  • Engage in bidirectional scientific and medical information exchange with Scientific Leaders
  • Provide balanced, factual scientific information on non-product areas and respond to scientific questions about company products
  • Develop professional relationships with national and regional Scientific Leaders
  • Conduct peer-to-peer scientific discussions and maintain reliable medical contact with Scientific Leaders
  • Address scientific questions and direct out-of-scope inquiries to appropriate company resources
  • Maintain current knowledge of the scientific and clinical environment in the therapeutic area
  • Initiate discussions with Scientific Leaders and potential investigators regarding research strategies, 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 and support protocol leadership with GCTO
  • Address investigator questions and provide information about company-sponsored clinical studies
  • Engage in scientific congresses and medical meetings and facilitate scientific/data exchange
  • Gather feedback and insights about medical or scientific needs, priorities, and concerns of Scientific Leaders and patients
  • Serve as a role model and support onboarding and sharing of therapeutic expertise
  • Contribute to an environment of belonging and empowerment

Requirements

What you’ll need
  • PhD, PharmD, DNP, DO, or MD
  • 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
  • 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
  • Consistent adherence to field and corporate policies, GMSA strategy, field SOPs, GCP guidelines, and administrative/operational responsibilities
  • Candidates must reside within IN, KY, WV, or VA
  • Ability to travel up to 50% within the territory
  • Valid driving license
  • No visa sponsorship available
  • Preferred: field-based medical experience, with GYN Oncology strongly preferred
  • Preferred: research experience
  • Preferred: demonstrated record of scientific/medical publication

Benefits

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