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SPC Global Medical Director - Ophthalmology

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Sanofi

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Location:
United States , Cambridge, MA / Morristown, NJ

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Category:
IT - Administration

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Contract Type:
Not provided

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Salary:

178500.00 - 297500.00 USD / Year
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Job Description:

Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. As Global Medical Director – Ophthalmology, you will play a pivotal role in shaping and executing the global medical strategy for our ophthalmology portfolio. This position requires strong scientific expertise, strategic leadership, and cross-functional collaboration to advance medical understanding, evidence generation, and external engagement. You will serve as a key medical representative and ensure alignment of medical activities with overall business objectives.

Job Responsibility:

  • Serve as the medical representative, providing strategic input and ensuring alignment of ophthalmology medical tactics with overall brand objectives
  • Participate in cross-functional workstreams to design and implement global medical programs supporting the ophthalmology portfolio
  • Contribute to the Global Medical Affairs Plan for ophthalmology assets
  • Collaborate with Scientific Communications to develop high-quality materials for external medical engagement and deliver global medical training programs
  • Lead and execute global medical activities within the Medical Affairs Plan, including advisory boards, expert meetings, and symposia
  • Drive evidence generation initiatives (e.g., Investigator-Initiated Studies, Real-World Evidence projects) in line with the Integrated Evidence Generation Plan (IEGP)
  • Lead strategically assigned projects to advance scientific understanding and clinical application of ophthalmology therapies
  • Build and maintain strong KOL relationships globally
  • Ensure cross-functional collaboration with Commercial, Regulatory, Pharmacovigilance, and Market Access teams
  • review promotional and non-promotional materials in Veeva/PromoMats
  • Support data dissemination strategy, including publications, congress planning, and scientific communication
  • Contribute to annual and long-term congress strategy, including symposia, abstracts, and scientific sessions
  • Maintain regular interaction with local medical teams in priority markets
  • Provide medical support to R&D, Pharmacovigilance, and Regulatory functions, including risk management and health authority interactions

Requirements:

  • Advanced degree (MD, PhD, PharmD) required
  • board certification (or eligible) in ophthalmology highly preferred
  • Minimum of 3 years of retinal disease expertise
  • at least 3 years of pharmaceutical/biotechnology industry experience preferred
  • Demonstrated experience in medical affairs or clinical development roles, including early pipeline management, KOL engagement, and scientific communication
  • Proven track record at country or global level
  • US market experience strongly preferred
  • Broad understanding of the drug development process, regulatory requirements, risk management, health authority interactions, and market access considerations
  • Expertise in retinal clinical science, therapeutic landscape, and evidence generation methodologies, including clinical trials and real-word evidence
  • Significant experience working with Research, Clinical Development, Commercial, Health Economic Value & Access teams
  • Demonstrated proficiency in scientific communication, publication planning, and congress strategy
  • Familiarity with compliance frameworks and promotional/non-promotional material review systems (e.g. Veeva/PromoMats)
  • Ability to define and execute global medical strategies
  • Skilled at building consensus across diverse stakeholders and geographies
  • Strong judgment in complex, matrixed environments
  • Experience mentoring and guiding teams or cross-functional groups
  • Ability to lead through ambiguity and drive innovation in medical affairs

Nice to have:

  • board certification (or eligible) in ophthalmology
  • US market experience
What we offer:
  • high-quality healthcare
  • prevention and wellness programs
  • at least 14 weeks’ gender-neutral parental leave
  • opportunities for career growth and development
  • promotion or lateral move opportunities, at home or internationally

Additional Information:

Job Posted:
January 10, 2026

Expiration:
April 01, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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