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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 and executing product plans, engaging stakeholders, and leading cross-functional initiatives. Proficient in scientific writing, regulatory compliance, and mentoring within a complex healthcare environment.
Highest-signal resume keywords
MD/PharmD/PhD Or Advanced DegreeMedical Affairs ExperienceScientific Writing SkillsLeadership And MentoringHealthcare Systems Knowledge
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Medical WritingQuantitative AnalysisQualitative AnalysisRegulatory ComplianceContent DevelopmentProject ManagementPromotional ReviewOutcomes ResearchCross-Functional CollaborationStrategic Planning
Soft Skills
Communication SkillsOrganizational SkillsProblem-Solving SkillsNetworking SkillsMulti-Tasking Skills
Industry Keywords
Healthcare SystemsPayer ProcessTherapeutic AreasGlobal Medical AffairsScientific ExchangeStakeholder EngagementCross-Functional InitiativesSOP DevelopmentMedical InformationCompliance Matters
About the role
Key responsibilities & impact- Shape and inform V&I Plans and the Scientific Platform
- Create, adapt, prioritize, and execute annual GSVC product plans aligned with V&I plans and the Scientific Platform
- Engage stakeholders and incorporate medical insights into product plans
- Lead development, review, approval, and communication of GSVC content
- Develop or delegate medical information letters, FAQs, disease- and product-related slide decks, congress booth materials, and digital/web-based medical content
- Review materials for scientific accuracy, relevance, appropriate literature, internal information, and company standards
- Engage stakeholders in content development, review, and approval, including CRT prioritization and reviewed-content management for the Payor team
- Communicate approved content to Medical Information and Global Medical and Scientific Affairs stakeholders
- Create globally leveraged materials with Outcomes Research and translate payer-landscape requirements
- Serve as a subject-matter expert and lead complex product-related projects and initiatives
- Mentor and empower GSVC P3/P4 staff and newly hired V&I GMVC team members
- Lead internal training on GSVC disease and product content
- Partner globally with Publications, Medical Directors, Payor & Health System Medical Affairs, Compliance, PDT, Outcomes Research, MSLs, and other stakeholders
- Lead complex cross-functional initiatives and departmental process improvements
- Author and update SOPs and lead organization or cross-organization initiatives
- Coordinate coverage and participate as a medical writer for Global Input Meetings
- Provide strategic guidance on complex issues, escalations, regulatory/compliance matters, and team objectives
- Conduct quantitative and qualitative analyses and report insights
- Lead onboarding and training for core functions
- Endorse change and foster innovation and cross-functional collaboration
Requirements
What you’ll need- MD/PharmD/PhD plus minimum five years of relevant Medical Affairs experience; OR MSN, BS degree in Pharmacy, MS degree in Life Sciences plus minimum 10 years of relevant Medical Affairs experience; OR BS degree in Nursing or Life Sciences plus minimum 15 years of relevant Medical Affairs experience
- Extensive knowledge of healthcare systems and payor process/environment
- Relevant working experience in Medical Affairs or Outcomes Research in the pharmaceutical industry
- Leadership through initiatives, mentoring, process improvements, and innovation
- Strong scientific writing and verbal communication skills
- Ability to network, prioritize, and collaborate cross-functionally
- Organizational and prioritization skills
- Multi-tasking and problem-solving skills
- Advanced degree preferred
- Exposure to global health systems and payer organization subject matter expertise
- Experience leading multiple Global or Regional Medical/Scientific Affairs Plans
- Experience with promotional review or medical/legal review activities
- Ability to develop or deliver scientific content for scientific exchange with external customers
- Ability to negotiate with cross-functional teams
- Experience working across geographies with different regulation/compliance requirements
- Extensive knowledge across multiple related therapeutic areas
- Strong analytical skills and ability to translate strategy into action plans
- Strong mentoring track record
- Ability to operate effectively in a complex, global, team-oriented organization
- No visa sponsorship
- Must be a US or Puerto Rico resident
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 days
- Sick days
- Hybrid work arrangement
- 10% travel