AI Deployment Manager (Content Development)

Summary:

Our client, a biopharmaceutical company based in Dublin, is seeking an AI Deployment Manager (Content Development) to drive the deployment of AI-enabled solutions across Centralised Content projects. The role will focus on improving content creation, content reuse and localisation through the evaluation, design and implementation of AI-enabled tools and workflows.

Responsibilities:

• Manage the pilot of generative AI solutions for creating first drafts of strategic story decks, congress updates and other priority content.
• Assess suitable tools, define priority use cases and evaluate opportunities to improve the efficiency and quality of content development.
• Develop a modular content plan and reusable content architecture for content, claims and approved content blocks.
• Define tagging, maintenance and reuse principles to enable faster adaptation of approved content across markets and channels.
• Define and test an AI-enabled localisation solution for approved GSL materials following Velocity implementation.
• Assess AI-supported translation capabilities and improve the findability of approved source materials, including through ARI.
• Collaborate with the Centralised Content team and relevant stakeholders to ensure solutions are practical, scalable and aligned with governance and approval workflows.
• Document findings, recommendations and implementation requirements, and communicate progress to key stakeholders.
• Identify opportunities to improve content supply chain efficiency through automation, standardisation and responsible use of AI.

Qualifications & Experience:

• Experience in content operations, content supply chain, digital transformation or AI-enabled workflow implementation.
• Experience evaluating or implementing AI, automation or generative AI solutions.
• Understanding of content modularisation, content reuse and localisation processes.
• Experience in the pharmaceutical, healthcare or life sciences sector would be advantageous.
• Knowledge of regulated content, scientific communications and approval workflows would be an advantage.