2 часа назад
GRA Global AdPromo Excellence Lead
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
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 initiatives across the GRA Advertising and Promotion organization with an accent on compliant communication, process quality, and digital transformation. Focus on reviewing promotional content, advising stakeholders on evolving advertising requirements, evaluating Gen AI tools, and maintaining regulatory KPIs, training materials, and governance documentation.
Location: Hybrid role based in Morristown, New Jersey or Cambridge, Massachusetts, United States
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines, vaccines, medical devices, and diagnostic products.
What you will do
- Review global promotional and non-promotional materials, product and disease communications, websites, and social media for regulatory compliance.
- Advise global business units and local affiliates on promotional activities, advertising requirements, industry trends, enforcement actions, and complaints.
- Support transformation programs, cross-functional initiatives, digital tool evaluations, and Gen AI use cases.
- Coordinate with transversal partners and regional teams and prepare stakeholder meeting materials and communications.
- Support gap analyses, KPI dashboards, best-practice documentation, process updates, SOP revisions, and governance activities.
- Maintain global training materials and conduct upskilling sessions for regional regulatory teams on digital initiatives.
Requirements
- Bachelor’s degree in Pharmaceutical Sciences, Life Sciences, or a related discipline; other degrees may be considered with relevant experience.
- At least 2 years of biopharmaceutical industry experience in regulatory affairs advertising and promotion review.
- Understanding of global codes and standards, including EFPIA and IFPMA, and the ability to review promotional content against them.
- Ability to interpret clinical data, medical publications, disease states, mechanisms of action, clinical trial design, and statistical concepts.
- Understanding of branded content, disease awareness materials, medical congress content, local SmPC information, and compliant messaging.
- Fluent English is required. Additional languages are beneficial.
Nice to have
- Experience with digital transformation initiatives, Gen AI, Modular Content, Core Claims, or MLR programs.
- Familiarity with Veeva, Microsoft Office, SharePoint, and other digital platforms.
Culture & Benefits
- Supportive, future-focused environment centered on scientific innovation and improving patient outcomes.
- Opportunities for career growth through promotion or lateral and international moves.
- Health and wellbeing benefits, including healthcare, prevention and wellness programs.
- At least 14 weeks of gender-neutral parental leave.
- Work at the intersection of AI, data, digital platforms, and biopharmaceutical research.
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