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Sanofi

Medical Director, Immunology

Sanofi

. Develop and execute an integrated U.S.

Posted 10/26/2026full-timeUnited StatesLead💰 $178,500 - $257,833 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in developing and executing integrated medical plans, managing clinical trials, and aligning medical strategies with commercial objectives. Proven ability to lead cross-functional teams and communicate effectively with stakeholders in the healthcare landscape.

Highest-signal resume keywords
Medical Affairs ExperienceClinical Trial DesignStakeholder ManagementRegulatory KnowledgeLeadership Presence

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
Clinical ResearchMedical Strategy DevelopmentEvidence SynthesisData AnalyticsGCP/ICH ComplianceMedical EducationHealth EconomicsPharmacovigilanceClinical Data InterpretationTrial Management
Soft Skills
Interpersonal SkillsProblem-SolvingAnalytical SkillsCommunication SkillsPresentation Skills
Tools & Technologies
AI ApplicationsReal World Evidence StudiesStatistical Analysis PlansMedical Communication ToolsProject Management Software
Industry Keywords
Allergy/ImmunologyHealthcare SystemsMedical LandscapePayer EnvironmentPublic HealthLife Cycle ManagementChange ManagementCultural CompetenceEthics in ScienceNorth America Residency

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Develop and execute an integrated U.S. Medical Plan covering Medical Education, Medical Communications and Publications, Health Outcomes, Safety, and Clinical Research
  • Manage the annual medical-plan budget
  • Translate medical strategy into actionable tactical plans and communicate progress to leadership, the Core Team, and execution partners
  • Align medical strategy with clinical development and commercial objectives and local U.S. needs
  • Provide medical leadership and scientific input to Clinical, Commercial, Market Access, Regulatory, and Sales functions
  • Partner with Field Medical, HEVA, Market Access, Marketing, Legal, and Regulatory teams
  • Address evidence gaps and payer-relevant data needs with the health economics team
  • Manage high-level external stakeholder relationships and support medical engagement planning and budget oversight
  • Support U.S. Phase IIIB–IV clinical programs, including protocol development, case report forms, statistical analysis plans, and study-data reporting
  • Oversee clinical studies in compliance with GCP/ICH guidelines and company standards
  • Review and approve Investigator Sponsored Trial concepts and protocols
  • Identify post-marketing clinical trial and registry needs and oversee execution
  • Ensure trial data are publicly disclosed accurately, timely, and in a balanced manner
  • Develop research collaboration opportunities addressing key clinical questions
  • Lead AI and advanced data analytics applications for evidence synthesis, signal detection, and unmet-needs identification
  • Guide evaluation and adoption of AI-driven approaches to literature analysis, clinical data interpretation, and scientific communication
  • Oversee design, generation, and integration of Real World Evidence studies into the U.S. medical plan
  • Build relationships with Key Opinion Leaders, researchers, and clinical experts
  • Lead medical and scientific advisory boards
  • Represent Sanofi at medical congresses, advisory boards, and scientific meetings
  • Provide disease-state and product training
  • Review and approve promotional, medical, regulatory, safety, scientific, and commercial materials for compliance and scientific accuracy
  • Review independent medical education grant applications and employee training materials
  • Partner with U.S. Drug Safety on adverse-event management, post-marketing surveillance, and safety-signal communication
  • Identify and escalate Product Alerts with Drug Safety, USRAMP, and Global Medical Affairs

Requirements

What you’ll need
  • Advanced Practice Provider with minimum 5 years of relevant clinical experience in allergy/immunology or advanced degree (NP, PA), or minimum 5 years of Medical Affairs experience in allergy/immunology strongly preferred
  • Industry experience in Medical Affairs and/or Clinical Development preferred
  • Significant experience in Medical Affairs Launch and Life Cycle Management activities preferred
  • High degree of knowledge of relevant healthcare systems, medical landscape, regulatory and payer environment, public health, and industry trends
  • Strong track record developing and executing medical strategies in the US preferred
  • Sound scientific and clinical judgment
  • In-depth understanding of conceptualizing, designing, and conducting clinical trials
  • Experience in clinical trial design and execution preferred
  • Ability to translate innovative strategies or solutions into actionable plans
  • Knowledge of general business practice, industry, medical practice, and Sanofi strategic objectives
  • Effective internal and external stakeholder management and cross-functional collaboration
  • Broad leadership experience and leadership presence
  • Ability to influence decision-making without authority in a complex, matrix environment
  • Ability to communicate scientific and medical data to internal and external stakeholders
  • Strong interpersonal, problem-solving, analytical, written, oral, and presentation skills
  • Highest personal integrity and commitment to ethics and scientific standards
  • Understanding and success in dealing with different cultures
  • Proven time and project management skills, prioritization, and expectation management
  • Knowledge of pharmacovigilance and local regulatory process
  • Proven record of successful change management
  • Digital literacy
  • Ability to travel up to 35% of the time
  • Required residency eligibility: US and Puerto Rico Residents Only / North America Applicants Only

Benefits

Comp & perks
  • Rewards package recognizing contribution and impact
  • Health and wellbeing benefits
  • High-quality healthcare
  • Prevention and wellness programs
  • At least 14 weeks’ gender-neutral parental leave
  • Opportunities for talent growth and career development through promotion or lateral moves
  • Opportunities to work at home or internationally
  • Patient insights incorporated into drug development and study design
  • Work with cutting-edge AI, data, and digital platforms