GRA Global AdPromo Excellence Lead
SanofiAbout the role
Job title: GRA Global AdPromo Excellence Lead
Location: Morristown, NJ - Cambridge, MA
About the job
A hybrid role combining support for global promotional material regulatory review (30%) with transversal excellence activities (70%). The position supports innovation, and operational efficiency across the GRA Advertising and Promotion (GRA AdPromo) organization while maintaining hands-on review expertise to ensure strategic initiatives remain grounded in operational realities.
Join the engine of Sanofi’s mission — where deep immunoscience 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 that treat and protect millions of people around the world and are supported and enhanced through our diverse portfolio of medical device and diagnostic products. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:
Global AdPromo Regulatory Review (~30%)
Work closely with the assigned global business units (commercial and medical) in the development of promotional / non-promotional materials, their review and prior approval. This also includes the review of internal and external documents issued by communication when related to products/diseases.
Act as an advisor for the team regarding the review of promotional activities on global level and/or for the local affiliates;
Review the regulatory aspects (as indicated in the Sanofi Global internet rules) of internet websites and social media (global).
Define the minimal quality standard and processes to be applied worldwide. Support the set up of guidelines / Quality documents on topics related to regulatory requirements around promotional aspects to ensure appropriate communication to the relevant stakeholders;
Advise teams on evolving regulatory requirements, industry trends, enforcement actions and complaints related to pharmaceutical advertising and promotion
Excellence Support Activities (~70%)
Innovation & Transformation Support
Represent GRA AdPromo in transformation programs and cross-functional initiatives
Support the evaluation and testing of digital tools and Gen AI use cases under guidance from the Excellence Head
Help compile data and observations for system and process reviews
Stakeholder Coordination
Support coordination activities with transversal partners and regional teams
Assist in preparing materials and communications for stakeholder meetings and updates
Advocate for the AdPromo team's strategic value and priorities
Operational Excellence Support
Assist with data collection and documentation for gap analyses of regulatory processes
Support maintenance of KPI reporting and dashboards by gathering and organizing relevant data
Help document best practices, process updates, and SOP revisions under senior guidance
Training & Capability Building Support
Assist in the preparation process documentation for both transversal and regulatory
Help maintain and update global training materials
Conduct upskilling sessions with (regional) regulatory teams on digital initiatives
Governance & Ways of Working Support
Provide administrative and coordination support for GRA AdPromo Governance activities
Assist in team engagement activities such as town halls and workshops
About you
Education
BA/BS degree in Pharmaceutical Sciences, Life Sciences, or related discipline required (other degrees considered with relevant experience)
Experience
2+ years of experience in the biopharmaceutical industry performing regulatory affairs advertising and promotion review
Required Skills
Good understanding of global codes and standards including ability to review against the EFPIA and IFPMA standards
Interpret complex clinical data (eg, CSRs, medical publications)
Posses
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