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Sanofi

Global pharma company; vaccines and R&D

Medical Director One Rare

Biology & BiotechPosted on Nov 12
Full-timeToronto, ON, CanadaCA$144.1k - CA$208.2k

About the Job

Requirements

  • An MD, PhD, PharmD, or equivalent advanced scientific or medical degree is required.
  • At least 5–8 years of experience in the pharmaceutical or biotechnology industry, including at least 7 years in medical affairs, medical education, or related fields.
  • Demonstrated experience in Rare Diseases and/or Rare Blood Disorders therapeutic areas, such as hemophilia, lysosomal storage disorders, metabolic diseases, or other rare conditions.
  • Proven people management experience with a track record of building, developing, and inspiring high-performing teams.
  • Deep understanding of the Canadian rare disease landscape, including Health Canada regulations, health technology assessment processes (CDA, INESSS), provincial reimbursement pathways, and patient access challenges specific to rare and ultra-rare conditions.
  • Strong scientific acumen and ability to translate complex rare disease data into clear, actionable medical strategies.
  • Communication, presentation, and stakeholder engagement skills to connect with specialists, patient advocates, payers, and regulators.
  • Proven experience working with external partners through a distribution model.
  • Bilingualism in English and French is a strong asset given the Canadian market context.

Responsibilities

  • Define and lead the Canadian medical affairs strategy for Rare Diseases and Rare Blood Disorders, aligned with global and regional priorities.
  • Develop and execute the Medical Affairs Plan for all assigned therapeutic areas within the One Rare portfolio.
  • Serve as the primary Canadian medical expert and scientific voice for the One Rare franchise, representing Sanofi’s scientific leadership internally and externally.
  • Contribute to lifecycle management strategies, pipeline development, and launch readiness activities for current and future rare disease and rare blood disorder assets.
  • Provide strategic medical input into brand planning, market access strategies, and reimbursement submissions.
  • Support development of diagnostic and treatment pathways to improve early identification, timely diagnosis, and optimal management of patients living with rare and ultra-rare conditions.
  • Build and maintain trusted, long-term relationships with partners.
  • Lead, coach, and develop a team of direct reports covering Rare Diseases and Rare Blood Disorders across Canada.
  • Set clear objectives aligned with medical and organizational priorities, provide regular constructive feedback, and support each team member’s career development and growth.
  • Foster a high-performance, inclusive, patient-centric team culture grounded in empathy, scientific rigor, and shared purpose.
  • Manage team resources, workload allocation, and performance reviews fairly and transparently.
  • Build and maintain relationships with key opinion leaders, rare disease specialists, metabolic disease centers, hemophilia treatment centers, academic institutions, patient advocacy groups, and healthcare professionals across Canada.
  • Lead and support advisory boards, scientific symposia, medical education initiatives, and patient and caregiver education programs.
  • Represent Sanofi at national and international medical congresses, rare disease forums, hemophilia conferences, and patient advocacy events.
  • Engage with Health Canada, Canadian Blood Services, CDA, INESSS, and provincial payer bodies on scientific and medical matters relevant to the One Rare portfolio.
  • Partner with rare disease and hemophilia patient advocacy organizations to integrate patient and caregiver perspectives into medical strategy and decision-making.
  • Oversee design and execution of local evidence generation activities, including investigator-initiated trials, patient registries, real-world evidence studies, and patient-reported outcomes research.
  • Support Canadian participation in global rare disease registries and natural history studies.
  • Ensure timely, accurate, and compliant dissemination of clinical and scientific data to relevant stakeholders.
  • Review and approve medical content, including publications, scientific slide decks, medical information responses, and patient and caregiver materials, for scientific accuracy, balance, and compliance.
  • Partner with Commercial, Market Access, Regulatory, Patient Safety, and Patient Advocacy teams on integrated, patient-focused strategies across the One Rare portfolio.
  • Collaborate with global and regional Medical Affairs teams to align priorities, contribute Canadian insights, and leverage global scientific resources.
  • Provide medical and scientific guidance for reimbursement submissions, health technology assessments, and compassionate or special access programs for rare disease patients.
  • Work with cross-functional teams to optimize patient support programs, access pathways, and continuity-of-care initiatives.
  • Ensure medical activities comply with Sanofi policies, Health Canada regulations, the Innovative Medicines Canada Code of Ethical Practices, and applicable laws and guidelines.
  • Champion ethics, integrity, patient safety, and transparency within the team and across external engagements.
  • Ensure adherence to pharmacovigilance requirements and timely adverse-event reporting under Sanofi’s safety obligations.
  • Serve as the primary medical point of contact for Canadian distributor partnerships related to rare disease and rare blood disorder medicines.
  • Act as the key medical liaison between Sanofi and its distributor to align medical strategies, scientific communication, and patient access.
  • Provide medical oversight and guidance to distribution partners to ensure consistent, accurate, and compliant medical information and support in interactions with healthcare professionals and patients.
  • Collaborate with distributors on medical education, training, and scientific communication activities aligned with Sanofi’s medical strategy and standards.
  • Review and approve medical content developed by or for distribution partners for scientific accuracy, balance, and compliance with Health Canada regulations and Innovative Medicines Canada guidelines.
  • Ensure alignment of medical strategies and messaging between Sanofi and distribution partners, particularly for rare disease treatment protocols and patient management guidelines.
  • Support distributor partners in addressing medical inquiries and adverse-event reporting, and in meeting pharmacovigilance requirements, with timely and compliant escalation.
  • Monitor and evaluate the quality of medical support through distributor partnerships and identify opportunities for continuous improvement and capability building.
  • Facilitate knowledge transfer and capability building with distributor medical teams so they can support healthcare professionals and patients with scientific rigor and compassion.
  • Travel approximately 30–40%, including domestic and international travel to congresses, advisory boards, educational events, and internal leadership forums.

Desired Qualifications

  • Experience working with hemophilia treatment centers or rare disease centers of excellence.
  • Knowledge of enzyme replacement therapies, substrate reduction therapies, gene therapies, or other novel rare disease modalities.
  • Experience with patient registries, natural history studies, or real-world evidence generation in rare disease settings.
  • Familiarity with compassionate access programs and special access pathways in Canada.

About the Company

Sanofi

Global pharma company; vaccines and R&D

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company size
10,001+
Company stage
IPO
Headquarters
Paris, France
Founded
1973

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