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Director, Medical Affairs – EMEA
Tandem Diabetes Care. Serve as a key scientific and medical expert for the EMEA region .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Medical Affairs leadership within the medical device and pharmaceutical industries, with a strong focus on evidence generation strategies, regulatory compliance, and market access initiatives across the EMEA region. Proficient in translating complex scientific information into actionable insights and fostering relationships with key stakeholders in healthcare.
Highest-signal resume keywords
Medical Affairs Leadership ExperienceEuropean Medical Device RegulationsEvidence Generation StrategiesFluency in English and Additional European LanguageAdvanced Degree in Scientific or Clinical Field
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Evidence GenerationHealth Technology AssessmentClinical Evidence InterpretationBiostatisticsMarket Access StrategiesRegulatory SubmissionsReimbursement PathwaysScientific Research MethodsDiabetes TechnologiesDigital Health Solutions
Soft Skills
Exceptional Communication SkillsCross-Functional CollaborationRelationship BuildingInfluencing Strategic DecisionsActionable Insights Translation
Certifications & Qualifications
Clinical Licensure (MD, RN, RD, NP)Advanced Degree (MS, MBA, PhD, MD, PharmD)
Industry Keywords
Medical DeviceMedTechPharmaceuticalEMEA RegionMarket LaunchesReimbursement InitiativesHealthcare Decision-MakingScientific OrganizationsKey Opinion LeadersMultinational Organizations
About the role
Key responsibilities & impact- Serve as a key scientific and medical expert for the EMEA region
- Partner with Clinical Affairs, Regulatory, Market Access, Marketing, Commercial, Commercial Excellence, and Operations teams
- Support product launches, reimbursement initiatives, and market expansion efforts
- Develop and execute the regional Medical Affairs strategy across EMEA
- Lead evidence generation initiatives supporting regulatory approvals, reimbursement, market access, healthcare decision-making, and product adoption
- Build relationships with key opinion leaders, healthcare providers, researchers, professional societies, academic institutions, investigators, and scientific organizations
- Deliver scientific presentations at conferences, advisory boards, webinars, and customer-facing events
- Provide medical and clinical expertise to field teams, distributor partners, and healthcare professionals regarding Tandem products and diabetes technology
- Translate scientific evidence into materials supporting regulatory submissions, reimbursement discussions, and market access activities
- Establish and support regional advisory boards and scientific exchange programs
- Monitor emerging clinical data, market trends, and scientific developments
- Partner with international investigators on research initiatives to generate evidence and support future market needs
Requirements
What you’ll need- Significant Medical Affairs leadership experience within the medical device, MedTech, or pharmaceutical industry
- Strong understanding of European medical device regulations, including EU MDR and CE Mark requirements
- Experience supporting market launches, reimbursement, market access, or expansion activities across multiple EMEA countries
- Expertise in evidence generation strategies, health technology assessment (HTA), payer evidence requirements, and reimbursement pathways
- Exceptional communication skills with the ability to translate complex scientific information into clear, actionable insights for diverse audiences
- Experience engaging healthcare professionals, investigators, and scientific thought leaders across international markets
- Fluency in English and proficiency in at least one additional European language; German particularly valued
- Advanced degree such as an MS, MBA, PhD, MD, PharmD, or equivalent scientific, clinical, or business qualification (preferred)
- Clinical licensure such as MD, RN, RD, NP, or another healthcare credential (preferred)
- Experience developing and leading Medical Affairs teams in an international environment
- Experience supporting diabetes technologies, digital health solutions, or other complex medical device portfolios
- Strong knowledge of scientific research methods, biostatistics, and clinical evidence interpretation
- Proven success influencing strategic decisions through data-driven insights and cross-functional collaboration
- Experience working within multinational organizations navigating diverse healthcare systems and reimbursement environments across EMEA
- Ability to travel extensively throughout Europe, approximately 50%
Benefits
Comp & perks- Workplace that celebrates achievements and supports employee well-being
- Growth-focused workplace with opportunities for professional development
- Inclusive and equal-opportunity work environment
- Referral program