Senior Program Manager; SPM; Mastocytosis

Senior Program Manager - Mastocytosis

Location:

Cambridge, MA

The Senior Program Manager (SPM) will drive business‑related initiatives within the Mastocytosis Therapeutic Area (TA), serving as a key operational partner to the Medical Program Lead (MPL) and the Mastocytosis Global Medical Team (GMT).

Working collaboratively with internal stakeholders and external Alliance partners (where applicable), the SPM will ensure seamless execution of lifecycle management (LCM) initiatives, launch deliverables, and strategic programs aligned with product development stages.

Operating within a dynamic matrix environment, the SPM will coordinate cross‑functional resources and activities to deliver on priorities outlined in the Global Medical Plans, ensuring strategic alignment and operational excellence across all TA‑specific initiatives.

Join the engine of Sanofi's mission, where deep immuno‑science meets bold, AI‑powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions.

We're an R&D‑driven, AI‑powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

• Lead program management initiatives for Mastocytosis in strategic partnership with the Medical Program Lead (MPL)
• Collaborate with Global Medical Director to operationalize Global Medical Team strategies and deliverables
• Drive integrated evidence generation planning through cross‑functional partnerships with Global Medical Directors, Brand teams, and functional leads

• Oversee comprehensive study lifecycle management, including process optimization, timeline coordination, and budget oversight for:
• Company‑Sponsored Studies (CSS):
  Manage approval process and serve as central Medical liaison for Clinical Sciences and Operations (CSO) communications and partnerships
• Investigator‑Sponsored Studies (ISS) & Real‑World Evidence (RWE):
  Partner with key stakeholders to capture operational details, study milestones, and budget requirements aligned with Medical plans
• Compliance & Reporting:
  Ensure adherence to study compliance requirements

• Optimize cross‑functional communication and decision‑making through meeting facilitation and stakeholder engagement
• Streamline operational workflows to ensure compliance with internal SOPs and external regulatory guidelines
• Utilize harmonized Program Management Tools to manage portfolio‑level activities across the Program Management organization

• Build and maintain strategic partnerships with internal teams and external collaborators
• Serve as primary advocate for alliance partner relationships (where applicable), ensuring alignment with collaboration objectives and deliverables
• Provide specialized program management support for Therapeutic Area‑specific initiatives and strategic priorities

• The ideal candidate brings a strong foundation in the biotech/pharmaceutical industry, combined with proven expertise in Project/Program Management. A scientific background and Medical Affairs experience are highly preferred.

• Bachelor of Science (BS) required
• Advanced degree in a scientific discipline strongly preferred

• Minimum 5 years of project/program management experience within biotech/pharma, clinical, or scientific environments
• Demonstrated ability to translate strategic objectives into actionable tactical plans
• Proven track record of managing complex, cross‑functional programs from initiation through completion with minimal supervision
• Medical Affairs experience preferred

• Deep understanding of project/program management methodologies, frameworks, and best practices
• Skilled in end‑to‑end project ownership, including scope, timelines, risk…