Associate Medical Director

Sanofi

. Support the development and execution of the Integrated Evidence Generation Plan and Global Medical Strategy for dupilumab in asthma and COPD .

Posted 10/2/2026full-timeUnited StatesLead💰 $148,500 - $214,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial methodology, design, and execution, particularly in Phase IV, observational, and real-world evidence studies. Strong ability to collaborate with cross-functional teams and maintain relationships with key opinion leaders in the respiratory and immunology fields.

Highest-signal resume keywords

Clinical Trial MethodologyPhase IV Study DesignScientific CommunicationExperience with DupilumabGlobal Medical Strategy

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignEvidence GenerationInterventional StudiesObservational StudiesReal-World Evidence StudiesBiologics ExperienceRespiratory TherapeuticsImmunology ExpertiseClinical DevelopmentResearch Evaluation

Soft Skills

Strong Presentation SkillsRelationship BuildingCollaborationPatient-Centric ApproachStrategic Insight Gathering

Certifications & Qualifications

Graduate Degree in Relevant Scientific Field

Industry Keywords

Pharmaceutical IndustryBiopharmaceutical IndustryBiotechnology IndustryMedical AffairsComplex Matrixed EnvironmentsAlliances and PartnershipsAsthmaCOPDKey Opinion LeadersPatient Associations

About the role

Key responsibilities & impact

Support the development and execution of the Integrated Evidence Generation Plan and Global Medical Strategy for dupilumab in asthma and COPD
Design clinical study synopses for Phase IV interventional, observational, and real-world evidence studies
Partner with regional and local affiliates to support evidence generation plans and studies aligned with the Global Medical Plan
Evaluate and support external sponsored research initiatives
Build and maintain relationships with respiratory experts, academics, patient associations, and key opinion leaders
Support advisory boards and roundtables to gather strategic insights
Ensure a patient-centric approach in the design and execution of clinical studies
Collaborate closely with the alliance to deliver shared objectives

Requirements

What you’ll need

Graduate degree in a relevant scientific or medical discipline (MD, PhD, PharmD, or Master's in a relevant scientific field)
Minimum of 5 years of industry experience in the pharmaceutical, biopharmaceutical, or biotechnology industry in R&D, Medical Affairs, or a related field
Experience operating within complex matrixed organizational environments
Strong scientific communication and presentation skills
Demonstrated experience in clinical trial methodology, design, and execution including Phase IV, observational, or real-world evidence studies
Experience in a global or regional medical or clinical development role
Experience in biologics within respiratory, immunology, or immune inflammation therapeutic areas
Experience with dupilumab, asthma, or COPD
Experience in alliance or partnership settings

Benefits

Comp & perks

Opportunities for growth and career development through promotion or lateral moves, at home or internationally
Rewards package recognizing contribution
High-quality healthcare
Prevention and wellness programs
At least 14 weeks’ gender-neutral parental leave
Employee benefit programs