Senior Program Manager (SPM) - Mastocytosis Employer Sanofi Location Cambridge, Massachusetts Start date Sep 5, 2026 View more categories View less categories Discipline Administration , Clinical , Medical Affairs , Science/R D , Project Management Required Education Bachelors Degree Position Type Full time Hotbed Genetown Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details Job title: Senior Program Manager -

Mastocytosis Location:

Cambridge, MA About the Job 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.

About Sanofi:

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 thattreat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main Responsibilities:

Strategic Partnership & Leadership 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 Study Lifecycle & Portfolio Management 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 Operational Excellence & Process Management 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 Stakeholder & Alliance Partner Engagement 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

About You Basic Qualifications:

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. Education Bachelor of Science (BS) required Advanced degree in a scientific discipline strongly preferred Experience 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 Core Competencies Program Management Excellence Deep understanding of project/program management methodologies, frameworks, and best practices Skilled in end-to-end project ownership, including scope, timelines, risk management, and budget oversight Proficient in developing and maintaining reporting dashboards with key performance metrics using harmonized organizational tools Leadership & Collaboration Demonstrated ability to lead and influence cross-functional teams within a matrix environment Strong management skills with the ability to engage effectively at all organizational levels Proven ability to foster a culture of teamwork, accountability, and collaboration Communication & Organization Exceptional interpersonal and communication skills, both written and verbal Highly organized with the ability to manage competing priorities and tight deadlines with professionalism and composure Comfortable operating in a fast-paced, dynamic environment with shifting priorities Technical Skills Advanced proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) Working knowledge of project/program management software (e.g., SharePoint Apps, MS Project, or equivalent tools) Why Choose Us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave. Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs. Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science. Help improve the lives of millions of people globally by making drug development quicker and more effective. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. #GD-SG #LI-GZ #LI-Onsite #vhd All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here. Company Pursue Progress. Discover Extraordinary. Science has been our calling from the beginning. Sanofi's heritage of turning the impossible into the possible stretches back to the 19th century — a rich history of healthcare innovation built by diverse companies united by one shared purpose. More than 150 years later, that spirit lives in everything we do and every person we serve — from the patients who take our medicines, to the healthcare professionals who trust us, to the 83,000+ employees and communities around the world who make it all possible. And today, we're writing the next chapter of that legacy. We are an R D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Better is out there. Better medications, better outcomes, better science. And it all starts with people like you — from different backgrounds, in different locations, doing different roles — united by a single mission: we chase the miracles of science to improve people's lives. Take the most important step in your career and help us change the lives of patients, families, and communities for the better. Company info Location Cambridge Massachusetts United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Site Head Portfolio Management Swiftwater, Pennsylvania Project Engineer (Biotech Focus) West Lebanon, NH MedSuRe Senior Manager, Program Delivery Rockville, MD