Director of Content Governance

6 days ago

London, Greater London, United Kingdom Advanced Accelerator Applications (Italy) - S... Full time
{"h1":{"text":"Associate Director of English"}},

The Global 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. 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.


Key Responsibilities:

  • 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.

Requirements:

  • Medical or science-related degree, MBA, or other business-related qualification. Content Approval Certifications are an advantage.
  • In-depth understanding of the operations of a pharmaceutical company including marketing, medical, value and access, commercial, compliance, digital/social media, content management and production.
  • Strong knowledge of compliance/regulatory requirements in the pharmaceutical industry and Novartis internal policies.
  • Strong policy, process, and project management skills.
  • Knowledge expert of Novartis compliance policies, procedures and how they apply to associates' roles and responsibilities.

Languages:

  • Fluent English (spoken and written).
  • Additional languages will be an advantage.

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