5 дней назад
GRA Global AdPromo Excellence Lead
122 250 - 176 583$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
GRA Global AdPromo Excellence Lead (Pharmaceutical Regulatory Affairs): Supporting global promotional material regulatory review and operational excellence across the GRA Ad-Promo organization with an accent on regulatory compliance, digital transformation, and cross-functional coordination. Focus on reviewing promotional content, evaluating AI-enabled tools, maintaining process dashboards, and strengthening global standards, training, and governance.
Location: Hybrid role based in Cambridge, Massachusetts or Morristown, New Jersey; US and Puerto Rico residents only
Salary: $122,250–$176,583.33 annually
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines, vaccines, medical devices, and diagnostic products.
What you will do
- Support global regulatory review and prior approval of promotional, non-promotional, website, social media, and disease-related communications.
- Advise global business units and local affiliates on advertising and promotion requirements, industry trends, enforcement actions, and complaints.
- Help define global quality standards, guidelines, regulatory processes, and SOP updates for promotional activities.
- Represent GRA Ad-Promo in transformation programs and cross-functional initiatives, including digital tools and Gen AI use cases.
- Coordinate stakeholder communications, KPI reporting, gap analyses, governance activities, workshops, and town halls.
- Maintain training materials and support upskilling sessions for regional regulatory teams on digital initiatives.
Requirements
- BA/BS in Pharmaceutical Sciences, Life Sciences, or a related discipline; other degrees are considered with 2+ years of relevant biopharma regulatory experience.
- At least 2 years of experience in biopharmaceutical regulatory affairs, advertising and promotion review, or a related function.
- Fluent English required.
- Understanding of global codes and standards, including EFPIA and IFPMA, and the ability to interpret clinical data and medical publications.
- Knowledge of pharmaceutical regulatory concepts, promotional review standards, compliant messaging, and local SmPC requirements.
- Strong attention to detail, organization, communication, collaboration, and adaptability.
Nice to have
- Experience with digital transformation initiatives such as Gen AI, Modular Content, Core Claims, or MLR programs.
- Familiarity with Veeva, Microsoft Office, SharePoint, and other regulatory technology systems.
- Additional language skills.
Culture & Benefits
- Supportive, future-focused environment centered on scientific innovation.
- Career growth opportunities through promotion or lateral moves, including international opportunities.
- Employee rewards and benefits package.
- Healthcare, prevention, wellness, and family benefits.
- Collaboration with science, clinical, and digital teams using AI, data, and digital platforms.
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