Senior Clinical Project Planner - Remote

Regeneron Pharmaceuticals

Armonk (NY)

Hybride

USD 115 000 - 187 000

Plein temps

Il y a 11 jours

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Résumé du poste

Regeneron Pharmaceuticals in Armonk, NY is seeking an accomplished Clinical Project Planning Manager to lead end-to-end study planning and scheduling for global trials. You will coordinate with Clinical Operations, Regulatory, and Program Leadership to deliver integrated project plans using Planisware Enterprise.

Responsibilities include developing cross-functional timelines, conducting critical path and risk analyses, presenting status updates to senior management, and ensuring data integrity

Qualifications

  • End-to-end clinical trial planning experience across Phases 1-4.
  • Proficiency with Planisware Enterprise and/or Orchestra.
  • Strong command of Microsoft Project, MS Office Suite, SharePoint, OnePager and OneNote.
  • Deep understanding of drug development including regulatory affairs and clinical supply management.
  • PMP or equivalent certification.

Responsabilités

  • Develop, implement, and maintain end-to-end cross-functional timelines from Phase 1 to NDA/BLA using Planisware or equivalent.
  • Perform critical path, schedule risk, and scenario analyses to identify risks and drive corrective actions.
  • Lead baseline and re-baseline processes with CDU and Program Leadership and ensure data integrity in planning workflows.
  • Influence cross-functional stakeholders, lead timeline review meetings, and present status updates to senior management.
  • Support planning activities across R&D programs and drive monthly planning close with IPPs.

Connaissances

End-to-end study planning
Cross-functional collaboration
Executive communication

Formation

BS degree

Outils

Planisware Enterprise
Orchestra
Microsoft Project
MS Office Suite
SharePoint
OnePager
OneNote

Description du poste

Regeneron Pharmaceuticals in Armonk, NY is seeking an accomplished Clinical Project Planning Manager to lead end-to-end study planning and scheduling for global trials. You will coordinate with Clinical Operations, Regulatory, and Program Leadership to deliver integrated project plans using Planisware Enterprise.

Responsibilities include developing cross-functional timelines, conducting critical path and risk analyses, presenting status updates to senior management, and ensuring data integrity

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