Associate Director, Content Approval for Vaccines – Posted Date: Feb 12 2026
As an Associate Director, Content Approval for Vaccines, you will play a pivotal role ensuring the global promotional and non‑promotional content meets the highest standards of quality, scientific accuracy, balance, and compliance. This includes adherence to internal GSK standards and applicable external regulations, including a robust understanding of the ABPI code of practice. The role will involve fostering robust relationships and collaborations within a highly matrixed environment that includes Commercial, Legal, Medical Affairs, Regulatory Affairs, Clinical Development, and third‑party suppliers at a global level.
Key Responsibilities
Primary medical reviewer and/or approver accountable for the thorough, timely review and approval of global promotional and non‑promotional materials.
Ensure content is scientifically accurate, meets scientific rigor, is fair‑balanced, and meets GSK requirements, standards, and processes while complying with applicable external regulations (incl. ABPI Code where relevant).
Maintain a deep understanding of the ABPI Code of practice (as an AQP), regulatory requirements, industry standards, best practices, and the GSK interpretation/position to ensure consistent application while reviewing and/or approving global medical or commercial content in scope of ABPI.
Have a strong understanding of business strategies/unmet needs to ensure content is aligned with current medical practices/guidelines and is fit for purpose for the targeted audience.
Work alongside MI counterparts and various business partners to align, validate, and identify solutions to ensure content is of the highest quality and relevant to the audience, supporting other GMI&CA team activities.
Serve as a key point of contact for regulatory and legal teams during audits and inspections, providing documentation and insights as needed.
Basic Qualifications & Skills
Master’s/Graduate Degree in Life Sciences or Healthcare.
Significant pharmaceutical industry experience.
Significant Medical Affairs experience as a reviewer of content used in promotional and non‑promotional settings.
Experience with commercial and medical activities from a global perspective in the pharmaceutical industry (e.g., promotion, medical education, external partnerships, advisory boards).
Strong understanding of content approval requirements, including external regulations (e.g., ABPI Code).
Strong understanding of international Codes of Practice – FDA, IFPMA, EFPIA, IPHA, ABPI, etc.
Experience with evaluation of clinical literature.
Preferred Qualifications & Skills
Experience working at both global and local country level.
Experience working with global teams in a matrix environment.
Experience in Vaccines.
Ability to accurately evaluate and summarize complex scientific literature, real‑world evidence, and other observational research studies for scientific evaluation needs by various customer types.
Closing Date for Applications : 26th of February (COB)
Please take a copy of the job description, as this will not be available post closure of the advert.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service, or any basis prohibited under federal, state or local law.
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