GRA Global AdPromo Excellence Lead
Sanofi
August 22, 2026
Remote friendly (Cambridge, MA)
United States
$122,250 - $176,583.33 USD yearly
Marketing
Main Responsibilities
Global AdPromo Regulatory Review (~30%)
- Work with global business units to develop promotional/non-promotional materials, including review and prior approval (including related internal/external communication documents).
- Advise on review of promotional activities globally and/or for local affiliates.
- Review regulatory aspects for global internet websites and social media.
- Define minimal quality standards and worldwide processes; support guidelines/quality documents for regulatory requirements.
- Advise on evolving regulatory requirements, industry trends, enforcement actions, and complaints.
Excellence Support Activities (~70%)
- Represent GRA AdPromo in transformation programs and cross-functional initiatives.
- Support evaluation/testing of digital tools and GenAI use cases.
- Compile data/observations for system and process reviews.
- Coordinate with transversal partners and regional teams; prepare stakeholder materials/updates.
- Assist with gap analyses of regulatory processes; support KPI reporting/dashboards.
- Document best practices, process updates, and SOP revisions under senior guidance.
- Maintain global training materials and support upskilling sessions for regional teams.
- Provide administrative/coordination support for governance activities and assist with team engagement.
Qualifications
- BA/BS in Pharmaceutical Sciences, Life Sciences, or related discipline (other degrees with relevant experience).
- 2+ years in biopharmaceutical industry performing regulatory affairs advertising/promotion review.
Required Skills
- Understanding of global codes/standards; ability to review against EFPIA and IFPMA.
- Ability to interpret complex clinical data (e.g., CSRs, medical publications).
- Scientific/clinical knowledge of disease states, mechanisms of action, clinical trial design, and statistical concepts.
- Use data and local SmPC for compliant messaging.
- Understand review standards for branded, disease awareness, and medical congress content.
Preferred Skills
- Experience with transversal/digital transformation (GenAI, Modular Content, Core Claims, MLR).
- Familiarity with regulatory tech systems (e.g., Veeva) and digital tools (Microsoft Office, SharePoint).
- Strong attention to detail, organization, communication, collaboration, adaptability.
Language
- Fluent English.
Benefits (explicit)
- At least 14 weeks’ gender-neutral parental leave; health and wellbeing benefits.
Compensation
- Determined commensurate with demonstrated experience.
Global AdPromo Regulatory Review (~30%)
- Work with global business units to develop promotional/non-promotional materials, including review and prior approval (including related internal/external communication documents).
- Advise on review of promotional activities globally and/or for local affiliates.
- Review regulatory aspects for global internet websites and social media.
- Define minimal quality standards and worldwide processes; support guidelines/quality documents for regulatory requirements.
- Advise on evolving regulatory requirements, industry trends, enforcement actions, and complaints.
Excellence Support Activities (~70%)
- Represent GRA AdPromo in transformation programs and cross-functional initiatives.
- Support evaluation/testing of digital tools and GenAI use cases.
- Compile data/observations for system and process reviews.
- Coordinate with transversal partners and regional teams; prepare stakeholder materials/updates.
- Assist with gap analyses of regulatory processes; support KPI reporting/dashboards.
- Document best practices, process updates, and SOP revisions under senior guidance.
- Maintain global training materials and support upskilling sessions for regional teams.
- Provide administrative/coordination support for governance activities and assist with team engagement.
Qualifications
- BA/BS in Pharmaceutical Sciences, Life Sciences, or related discipline (other degrees with relevant experience).
- 2+ years in biopharmaceutical industry performing regulatory affairs advertising/promotion review.
Required Skills
- Understanding of global codes/standards; ability to review against EFPIA and IFPMA.
- Ability to interpret complex clinical data (e.g., CSRs, medical publications).
- Scientific/clinical knowledge of disease states, mechanisms of action, clinical trial design, and statistical concepts.
- Use data and local SmPC for compliant messaging.
- Understand review standards for branded, disease awareness, and medical congress content.
Preferred Skills
- Experience with transversal/digital transformation (GenAI, Modular Content, Core Claims, MLR).
- Familiarity with regulatory tech systems (e.g., Veeva) and digital tools (Microsoft Office, SharePoint).
- Strong attention to detail, organization, communication, collaboration, adaptability.
Language
- Fluent English.
Benefits (explicit)
- At least 14 weeks’ gender-neutral parental leave; health and wellbeing benefits.
Compensation
- Determined commensurate with demonstrated experience.