Overview
As an Associate Director, Content Approval for Vaccines, 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 role involves fostering robust relationships 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 responsible for thorough, timely review and approval of Global promotional and non-promotional materials.
* Ensure content is scientifically accurate, rigorous, fair-balanced, and compliant with GSK standards and applicable external regulations (including ABPI Code where relevant).
* Maintain deep scientific and therapeutic expertise on assigned products and therapy areas.
* Understand ABPI Code of practice and GSK interpretation to ensure consistent application during review/approval of global content within ABPI scope.
* Align content with business strategies and guidelines to ensure it is fit for purpose for the targeted audience.
* Collaborate with MI counterparts and business partners to validate content quality and relevance.
* Provide timely feedback to content created/reviewed by third-party vendors; escalate when vendors do not meet quality standards.
* Escalate to leadership when content may pose business risk.
* Stay up to date with evolving regulatory requirements, industry standards, and best practices to ensure ongoing compliance.
* Identify issues and opportunities for continuous improvement in materials and activities.
* Serve as a point of contact for regulatory and legal teams during audits and inspections, providing documentation as needed.
* Participate in workstreams to develop best practices and continuous improvement for the content approval process.
* Contribute to content creation plans to ensure deliverables and timelines are realistic and achievable.
* Support other GMI&CA team activities and onboarding of new team members as required.
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 in promotional and non-promotional settings.
* Experience with global promotion/medical activities (promotion, medical education, external partnerships, advisory boards).
* Experience evaluating clinical literature.
Preferred Qualifications
* Strong understanding of content approval requirements and external regulations (e.g., ABPI Code).
* Understanding of international Codes of Practice (FDA, IFPMA, EFPIA, IPHA, ABPI).
* Ability to work under pressure and meet tight timelines.
* Experience working globally and in matrix environments; ability to collaborate effectively and foster teamwork.
* Experience in vaccines.
* Strong organizational and planning skills; clear and concise scientific communication.
* Customer-focused, problem-solving, and conflict resolution skills.
Why GSK? Visit the GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants receive equal consideration for employment without regard to race, color, religion, sex, national origin, age, disability, or any other basis prohibited by law.
Additional Information
* Seniority level: Not Applicable
* Employment type: Full-time
* Job function: Marketing, Public Relations, and Writing/Editing
* Industries: Pharmaceutical Manufacturing
Please note: If you require an accommodation or other assistance to apply for a job at GSK, contact the GSK Service Centre.
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