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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Medical Affairs with a strong focus on developing scientific content and training resources for payer and health systems. Proven ability to engage stakeholders, lead cross-functional teams, and ensure compliance with scientific communication standards.
Highest-signal resume keywords
Medical Affairs ExperienceScientific WritingProject ManagementHealthcare Systems KnowledgeHealth Economics Research
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Content DevelopmentMedical CommunicationsHealth Technology AssessmentEpidemiologyClinical PathwaysScientific Literature ReviewPayer ReimbursementOutcomes ResearchComplex Problem-SolvingStrategic Thinking
Soft Skills
Communication SkillsMentoringInnovationPrioritizationCollaboration
Certifications & Qualifications
MDPharmDPhD
Industry Keywords
Healthcare AccessRegulatory ComplianceScientific PresentationsGlobal Health SystemsMedical/Scientific Affairs
About the role
Key responsibilities & impact- Engage key stakeholders in executing the Value & Implementation Plan
- Develop payer and health systems scientific content and translate it into field-ready training, onboarding, and capability-building resources
- Create, adapt, and prioritize annual Global Scientific & Value Content plans
- Execute content plans covering medical information letters, verbal response documents, infographics, disease- and product-related slide decks, global congress medical booth materials, and digital/web-based medical content
- Develop payer and health systems scientific content for general medicine, specialty, vaccine, and infectious disease portfolios
- Support launches, anticipated approvals, guideline updates, Phase 3 data releases, non-interventional real-world evidence, Health Care Economic Information, and competitive intelligence
- Engage stakeholders in development, review, and approval of content; attend CRT prioritization meetings and support Medical Legal Review
- Monitor scientific, policy, methodological, and competitive developments
- Coordinate coverage for group input meetings and participate as a medical writer
- Translate scientific, value, and outcomes evidence into field-ready curricula and practical learning experiences
- Establish approval-readiness milestones, coordinate implementation timelines, and lead deployment of scientific training
- Support structured onboarding for new Payer & Health Systems colleagues
- Maintain, update, retire, reuse, and redeploy training resources
- Support performance measures for launch readiness, onboarding effectiveness, scientific exchange mastery, and training completion
- Serve as a therapeutic-area subject-matter expert and shape Value & Implementation strategy
- Translate scientific, clinical, HEOR, guideline, and access information into scientific content and actionable field resources
- Lead across matrixed teams, influence without direct authority, align stakeholders, and manage multiple priorities
- Lead departmental process-improvement initiatives and foster innovation and cross-functional collaboration
- Mentor newly hired Value & Implementation GMVC team members and facilitate onboarding and training for P3/P4 Global Scientific & Value Content team members
- Assist the Global Scientific & Value Content Team Lead in continued team development
Requirements
What you’ll need- MD/PharmD/PhD
- Minimum of five (5) years of relevant Medical Affairs experience
- Extensive knowledge of healthcare systems, payer processes and environments, and clinical pathways
- Relevant experience in Medical Affairs, Outcomes Research, health services research, epidemiology, health technology assessment, or a related pharmaceutical-industry field
- Strong scientific writing and communication skills
- Strategic thinking, project management, innovation, prioritization, and complex problem-solving skills
- Knowledge of manufacturer-initiated scientific communications guidance, including FDAMA 114, Scientific Information on Unapproved Uses, and Academy of Managed Care Pharmacy Real-World Evidence guidance
- Commitment to scientifically accurate, medically appropriate, and compliant communication
- Preferred: global health systems and payer organization expertise
- Preferred: experience leading multiple global or regional Medical/Scientific Affairs plans
- Preferred: promotional review or medical/legal review experience
- Preferred: record of scientific presentations or publications
- Preferred: experience across geographies with different regulatory and compliance requirements
- Preferred: extensive knowledge across multiple related therapeutic areas
- Preferred: strong mentoring track record
- Content Development
- Healthcare Access
- Health Economics Research
- Medical Communications
- Medical Knowledge
- Medical Literature Review
- Payer Reimbursement
- Professional Networking
- Project Management
Benefits
Comp & perks- Annual bonus and 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
- Hybrid work arrangement
- 10% travel requirement