Associate Director, Content Approval, Specialty / Gen Med

Job description

Site Name : USA - Pennsylvania - Upper Providence, Durham Blackwell Street, GSK HQ, Philadelphia Walnut Street, UK London New Oxford Street

Posted Date : Dec 4 2025

As an Associate Director, Content Approval for Specialty / Gen Med , you will play a pivotal role in 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. This role will involve fostering robust relationships and collaborations within a highly matrixed environment which includes but is not limited to Commercial, Legal, Medical Affairs, Regulatory Affairs, Clinical Development, and third‑party suppliers at a Global level.

Key Responsibilities

• Primary medical reviewer and / or approver who is accountable for the thorough, timely review and approval of Global promotional and non‑promotional materials.
• Ensure content is scientifically accurate, meets the scientific rigor (i.e., levels of evidence); is fair‑balanced and meets the GSK requirements / standards / processes as well as complies with applicable external regulations (incl. ABPI Code where relevant).
• Maintain deep scientific and therapeutic expertise on assigned products and therapy areas.
• Maintain a deep understanding of ABPI Code of practice (as an AQP / Appropriately Qualified Person) and the GSK interpretation / position to ensure consistent application while reviewing and / or approving global medical or commercial content in scope of ABPI.
• Strong understanding of the business strategies / unmet needs to ensure the content is aligned with current medical practices / guidelines, and the content is fit for purpose to the targeted audience.
• Work alongside various business partners to align, validate, and identify solutions to ensure content is of the highest quality and relevant to the audience.
• Provide timely feedback and recommendations for content created and / or reviewed by third‑party vendors and escape when third‑party vendors do not meet the quality standards.
• Address and / or escape to appropriate leadership when content may result in a risk to the business.
• Stay up to date with evolving regulatory requirements, industry standards, and best practices to ensure continuous compliance.
• Identify issues, themes and / or opportunities for continuous improvement that enhance the quality and compliance of materials and activities.
• Serve as a key point of contact for regulatory and legal teams during audits and inspections, providing documentation and insights as needed.
• Actively participate in workstreams to develop best practices, ways of working and continuous improvement for promotional and non‑promotional content approval process.
• Actively contribute and provide input to content creation plans to ensure content deliverables and timelines are realistic and achievable.
• Support other GMI&CA team activities (e.g., MI content creation, US medical review), when required and in onboarding new content approval team members.

Why You?

Basic Qualifications

Preferred Qualifications

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Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade. Our focus is on respiratory, immunology and inflammation; oncology; HIV; and infectious diseases.

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