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Associate Director, Content Review Process
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.Associate Director, Content Review Process Job ID: REQ-10007714Location: SpainDate: Sep 09, 2024Summary This role can be based in Barcelona, Spain or London, United Kingdom. Hybrid working model for both locations (12 days per month in the office).Note: Novartis is not able to offer relocation or visa support for this role: please only apply if this location is accessible for you and you have the right to work in the country you are applying to.The Global Content Review Process Associate Director (AD) will manage an external partner(s) who will perform a centralized content approval service, provide managerial directions, as well as ensure that an established review and approval process is followed on global and country level adhering to regulatory and legal requirements as well as internal policies.This role will oversee the medical approval process for promotional and educational materials in a global and local context. Collaboration with cross-functional teams to ensure timely approval of global content is key.The Content Review Process Associate Director plays a critical role in ensuring that promotional and educational activities and materials are approved in a timely and compliant manner while maintaining the highest standards of quality and safety. The AD will also be responsible for the Content Review Process ongoing monitoring and further refinement/improvement.About the Role Major accountabilities:Manage dedicated external partner for content approval, ensure adequate staffing for content approval team and ongoing performance management.Manage content standards - including updates of relevant guidelines and processes to ensure consistency and quality of reviews. Coordinate implementation, change management, communication, and business training plans across functions and geographies.Business partnership - by proactively solving bottlenecks and inefficiencies as it relates to content approval, while ensuring compliance of materials with global regulations and company policies.Be single point of contact and subject matter expert for content approval teams and provide guidance & support to the other departments on medical topics related to product promotion and marketing (e.G., medical, marketing, regulatory affairs, and clinical development).Manage training needs – including training programs for content creators, medical and commercial reviewers.Key performance indicators:Number of materials challenged/incompliant - per month.Business partnership satisfaction - quarterly surveys.Review and Approval timelines – per asset types/monthly.Minimum Qualifications:Medical or science-related degree, MBA, or other business-related qualification. Content Approval Certifications are an advantage.Preferred 5-6 years professional experience in the pharma industry
