OverviewAs an Associate Director, Content Approval for Vaccines, you will play a pivotal role in ensuring the global promotional and non-promotional content meets high 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 involves fostering robust relationships and collaborations within a matrixed environment including 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 scientific rigor (levels of evidence), is fair-balanced and complies with GSK requirements/standards/processes as well as 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 and the GSK interpretation/position to ensure consistent application when reviewing and/or approving global medical or commercial content within ABPI scope. Align content with business strategies/unmet needs to ensure it is fit for purpose for the targeted audience. Collaborate with MI counterparts and business partners 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 escalate when vendors do not meet quality standards. Address and/or escalate to appropriate leadership when content may pose 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 opportunities for continuous improvement that enhance 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. Participate in workstreams to develop best practices, ways of working and continuous improvement for promotional and non-promotional content approval process. Contribute input to content creation plans to ensure 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.

Basic Qualifications

Master’s/Graduate Degree in Life Sciences or Healthcare 4+ years of pharmaceutical industry experience 3+ years of Medical Affairs experience as a reviewer of content used in promotional and non-promotional settings Experience with global promotion, medical education, external partnerships, advisory boards Experience evaluating clinical literature

Preferred Qualifications

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) Ability to cope with pressure and meet tight timelines Experience working at both global and local country levels in matrix environments Strong organizational, planning, and collaboration skills Ability to work independently and manage multiple projects simultaneously Ability to evaluate and summarize complex scientific literature, real-world evidence, and other observational studies for scientific evaluation across customer types Clear and concise scientific communication Customer focus, problem solving, and conflict resolution skills

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 aimed at positively impacting health at scale, focusing on respiratory, immunology and inflammation; oncology; HIV; and infectious diseases. We strive to create an environment where people can thrive, with a culture of ambition for patients, accountability for impact and doing the right thing. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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, military service or any basis prohibited under federal, state or local law. #J-18808-Ljbffr