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 includes adherence to internal GSK standards and applicable external regulations, including a robust understanding of the ABPI code of practice.
Requirements
- 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 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
- Provide timely feedback and recommendations for content created and/or reviewed by third-party vendors and escalate when third-party vendors do not meet the quality standards
- Address and/or escalate 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.
Benefits
- Comprehensive benefits program
- Equal opportunity employer
- Accommodations for people with disabilities
