Associate Director, Content Approval, Vaccines - London
1 month ago
As an Associate Director Content Approval for Vaccines you will play a pivotal role in ensuring global promotional non-promotional content meets highest standards of quality scientific accuracy balance compliance.
This includes adherence to internal GSK standards applicable external regulations including robust understanding of ABPI code practice.
Primary medical reviewer approver accountable thorough timely review approval Global promotional non-promotional materials Ensure content scientifically accurate meets scientific rigor i.e levels evidence fair-balanced meets GSK requirements/standards/processes complies applicable external regulations incl ABPI Code where relevant Maintain deep therapeutic expertise assigned products therapy areas Maintain deep understanding ABPI Code practice AQP/Appropriately Qualified Person ensure consistent application reviewing approving global medical commercial content scope ABPI Work alongside MI counterparts various business partners align validate identify solutions ensure content highest quality relevant audience Provide timely feedback recommendations created reviewed third-party vendors escalate when vendors do not meet quality standards Address escalate appropriate leadership when content may result risk business Stay up date evolving regulatory requirements industry standards best practices ensure continuous compliance Identify issues themes opportunities continuous improvement enhance quality compliance materials activities Serve key point contact regulatory legal teams audits inspections providing documentation insights needed Actively participate workstreams develop best practices ways working continuous improvement promotional non-promotional approval process Actively contribute provide input creation plans ensure deliverables timelines realistic achievable Support other GMI&CA team activities e.g MI creation US medical review when required onboarding new approval team members.
Job description
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