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Sanofi

US Medical Director – Transplantation Kidney

Sanofi

. Develop and execute US medical strategy for transplant products, focusing on kidney transplantation and belumosudil (Rezurock) .

Posted 10/12/2026full-timeUnited StatesLead💰 $178,500 - $257,833 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in developing and executing medical strategies for transplant products, with a strong focus on kidney transplantation and the ability to collaborate across various stakeholders. Possesses advanced knowledge in medical affairs, clinical development, and regulatory compliance within the pharmaceutical industry.

Highest-signal resume keywords
Pharmaceutical Medical Affairs ExperienceAdvanced Degree (M.D., PhD., PharmD, DNP, MSc Pharm)Knowledge of Transplantation and Disease ProcessesClinical Trials and Retrospective Database AnalysisStakeholder Management and Interpersonal Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Medical Strategy DevelopmentClinical DevelopmentRegulatory ComplianceScientific Evidence GenerationData AnalysisEpidemiologyBiostatisticsHealth Economics/PolicyTransplant Market KnowledgeCompassionate Use Programs
Soft Skills
Exceptional Communication SkillsStrategic Problem-SolvingCustomer/Patient-Centric ThinkingInfluencing Without AuthorityAbility to Work in a Matrixed Environment
Industry Keywords
TransplantationPharmaceuticalsMedical AffairsClinical TrialsRegulatory DocumentsScientific ExchangeHealthcare DeliveryPromotional Materials ReviewEthical GuidelinesIndustry Compliance

About the role

Key responsibilities & impact
  • Develop and execute US medical strategy for transplant products, focusing on kidney transplantation and belumosudil (Rezurock)
  • Develop and execute an integrated medical affairs plan covering medical education, insight gathering, scientific evidence generation, publications, IME, advisory boards, and scientific information exchange
  • Identify and implement medical research projects, including Sanofi-sponsored, external stakeholder, and investigator-initiated projects
  • Represent medical perspectives in US regulatory and reimbursement documents and provide clinical insights for new business opportunities
  • Collaborate with global medical, commercial, regulatory, legal, scientific communications, pharmacovigilance, and public affairs stakeholders
  • Support healthcare professionals in optimizing patient care through evidence-based decisions
  • Coordinate US medical affairs functions, including Compassionate Use Programs, while maintaining integrity and compliance
  • Support Investigator Sponsored and Company Sponsored studies
  • Identify and oversee post-marketing data generation through RWE, registries, and external collaborations
  • Lead innovative solutions addressing unmet business needs
  • Develop scientific exchange resources for solid organ and stem cell transplantation
  • Translate field medical insights into strategy and action plans
  • Build and maintain relationships with thought leaders
  • Provide medical leadership to sales, marketing, legal, and regulatory functions
  • Review and approve promotional materials for medical accuracy
  • Communicate scientific knowledge and support optimal healthcare delivery and patient outcomes
  • Establish processes and venues for sharing information and best practices across internal customer segments and priority US markets
  • Demonstrate Sanofi values and support patient-centric medical strategies

Requirements

What you’ll need
  • At least 5 years of Pharmaceutical Medical Affairs or clinical development experience; academia experience considered
  • Advanced degree (e.g., M.D., PhD., PharmD, DNP or MSc Pharm with extensive therapeutic area experience)
  • Working knowledge of treatments, product labeling, and Federal Regulations pertaining to pharmaceuticals, promotion, and industry-sponsored scientific and educational activities
  • Strong literature knowledge of stem cell/bone marrow transplantation, common pathology, and disease processes
  • 5–10 years of professional experience involving transplant patients and/or collaboration with external professional associations and field-based teams
  • Experience with clinical trials, retrospective database analysis, and healthcare delivery in the United States and globally
  • Experience with biotechnology and drug development processes
  • Exceptional oral and written communication skills and ability to evaluate and communicate scientific data
  • Fluent English
  • Ability to influence without authority in a highly matrixed environment
  • Strategic problem-solving ability
  • Customer/patient-centric thinking
  • Stakeholder management and interpersonal skills
  • Ability to work in a matrixed environment
  • Working knowledge of epidemiology, biostatistics, and health economics/policy
  • Experience working on projects and/or operations within strict timeline and budget parameters
  • Knowledge of global and US transplant markets and stakeholders influencing medical decisions
  • Understanding of ethical guidelines and pharmaceutical-industry compliance requirements
  • Business acumen and understanding of economic, financial, and industry data
  • Travel requirement: 10–25%

Benefits

Comp & perks
  • Supportive, future-focused team
  • Opportunities for promotion or lateral career moves, at home or internationally
  • 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
  • Patient insights incorporated into drug-development studies
  • Equal Opportunity employer