Senior Program Manager (SPM), Immunology Medical Evidence Generation (MEG)/Life Cycle Management (LCM)
Sanofi
June 25, 2026
Remote friendly (Cambridge, MA)
United States
$122,250 - $176,583.33 USD yearly
Medical Affairs
Main Responsibilities
- Support building and execution of the Global Medical Affairs strategy and plan for Dupilumab related to Integrated Evidence Generation Planning (IEGP).
- Collaborate with Life Cycle Management (LCM) Leads to ensure synergy of IEGP development and associated financial planning.
- Apply a “Glocal” approach to country inclusion/exchange to identify and prioritize data gaps; enable two-way interaction between local entities and global medical stakeholders.
- Implement and execute operational aspects of Medical Evidence Generation across the dupilumab franchise: data gap generation/prioritization, Medical Brand Planning, IEGP implementation/maintenance, and financial documentation insight; align medical and financial planning for long-range forecasting.
- Coordinate evidence generation insights across affiliate Medical Directors to align evidence portfolio development across G10 countries and beyond.
- Collaborate with alliance partner Regeneron to define and maintain consistent evidence strategy with Research and Clinical Development stakeholders.
- Coordinate communication, alignment, and workshopping with cross-functional partners (including HEVA, Market Access, and Translational).
- Provide consistent strategy and evidence generation reporting to senior leadership and alliance meetings.
- Maintain and optimize Medical Program Management (MPM) tracking tools; ensure cross-functional representation, efficient/compliant workflows (internal SOPs and external guidelines), and harmonized program management tools.
Qualifications
- Bachelor of Science required; advanced science degree preferred; MBA a plus.
- 3+ years project/program management in biotech/pharma or clinical/scientific environment.
- Lead projects and translate strategy into tactical plans; strong understanding of PM methodologies.
- Coordinate cross-functional teams in a matrix environment; manage end-to-end with minimal supervision.
- Create reporting dashboards with key metrics; strong interpersonal/communication skills; strong organization; multitask and meet tight timelines.
- Exceptional MS Office; working knowledge of program/project management software.
Preferred Qualifications
- Biotech/pharma and direct Project/Program Management experience; scientific background and Medical Affairs experience preferred.
- Alliance environment experience; ability to work with Regeneron.
- Strong scientific data presentation and communication; interface with academicians/agencies/industry executives.
- Understanding of pharmaceutical/biotech drug development and commercialization; leadership, urgency, flexibility in changing environments.
Benefits
- Health and wellbeing benefits; high-quality healthcare and prevention/wellness programs; at least 14 weeks’ gender-neutral parental leave.
- Support building and execution of the Global Medical Affairs strategy and plan for Dupilumab related to Integrated Evidence Generation Planning (IEGP).
- Collaborate with Life Cycle Management (LCM) Leads to ensure synergy of IEGP development and associated financial planning.
- Apply a “Glocal” approach to country inclusion/exchange to identify and prioritize data gaps; enable two-way interaction between local entities and global medical stakeholders.
- Implement and execute operational aspects of Medical Evidence Generation across the dupilumab franchise: data gap generation/prioritization, Medical Brand Planning, IEGP implementation/maintenance, and financial documentation insight; align medical and financial planning for long-range forecasting.
- Coordinate evidence generation insights across affiliate Medical Directors to align evidence portfolio development across G10 countries and beyond.
- Collaborate with alliance partner Regeneron to define and maintain consistent evidence strategy with Research and Clinical Development stakeholders.
- Coordinate communication, alignment, and workshopping with cross-functional partners (including HEVA, Market Access, and Translational).
- Provide consistent strategy and evidence generation reporting to senior leadership and alliance meetings.
- Maintain and optimize Medical Program Management (MPM) tracking tools; ensure cross-functional representation, efficient/compliant workflows (internal SOPs and external guidelines), and harmonized program management tools.
Qualifications
- Bachelor of Science required; advanced science degree preferred; MBA a plus.
- 3+ years project/program management in biotech/pharma or clinical/scientific environment.
- Lead projects and translate strategy into tactical plans; strong understanding of PM methodologies.
- Coordinate cross-functional teams in a matrix environment; manage end-to-end with minimal supervision.
- Create reporting dashboards with key metrics; strong interpersonal/communication skills; strong organization; multitask and meet tight timelines.
- Exceptional MS Office; working knowledge of program/project management software.
Preferred Qualifications
- Biotech/pharma and direct Project/Program Management experience; scientific background and Medical Affairs experience preferred.
- Alliance environment experience; ability to work with Regeneron.
- Strong scientific data presentation and communication; interface with academicians/agencies/industry executives.
- Understanding of pharmaceutical/biotech drug development and commercialization; leadership, urgency, flexibility in changing environments.
Benefits
- Health and wellbeing benefits; high-quality healthcare and prevention/wellness programs; at least 14 weeks’ gender-neutral parental leave.