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AI / Digital Transformation, Regulatory Medical Writing Job at The Fountain Group

AI / Digital Transformation, Regulatory Medical Writing Job at The Fountain Group

MediabistroTitusville, NJ, United States
18 days ago
Job type
  • Full-time
Job description

Overview

We are currently seeking an AI / Digital Transformation, Regulatory Medical Writing for a prominent Pharmaceutical client. This position is Remote.

Job Details :

  • W2 only. No C2C.
  • Pay : 80.00-88.23 / hr.
  • Length of Assignment : 1 year to start with potential extension.
  • 100% remote role. No travel required. Must be able to work EST hours.
  • Department : Regulatory Medical Writing (RMW).

Responsibilities

We are seeking a skilled and experienced contractor to support the delivery of the AI strategy within Regulatory Medical Writing (RMW). This role will work closely with the RMW AI Business Leads to enable digitization, streamline document processes, and support the deployment of AI-powered solutions across the document lifecycle.

Support execution of the RMW functional AI strategy, including : Change management activities, AI quality improvement initiatives, coordination of user acceptance testing (UAT), and deployment of upgrades and expansion into new document types.

Contribute to the implementation of SubX capabilities (lean writing, storytelling, predictive text) by year-end 2026. Assist in the technical go-live and deployment of AI-enabled Document Generation solutions (1Q–3Q 2026).

Strong understanding of the RMW document landscape, including Clinical Study Reports (CSRs), narratives, and other regulatory deliverables.

Qualifications

  • Top Three Skills : Prove n Experience in Digital Transformation & AI-Enabled Workflows Demonstrated success in implementing GenAI or similar technologies for document authoring and automation. Experience with structured data workflows and process optimization in a regulated environment.
  • Top Three Skills : Strong Project Coordination & Change Management Capabilities. Ability to support cross-functional initiatives including user acceptance testing, deployment planning, and change enablement. Skilled in organizing and driving adoption of new tools and upgrades across diverse stakeholder groups.
  • Top Three Skills : Knowledge of Regulatory Medical Writing (RMW) Document Landscape. Hands-on experience with Clinical Study Reports (CSRs), patient narratives, and other regulatory deliverables. Familiarity with Regulatory Information Management systems and data-sharing platforms.
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    Medical Writing Job • Titusville, NJ, United States