Project Manager in United

Job Description

Role Summary

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Experienced project manager with regulatory domain expertise responsible for leading multiple concurrent regulatory information, data, and systems initiatives. This role will oversee system implementations, process transformation activities, and cross-functional coordination across business, regulatory, and technology teams.

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Key Responsibilities

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• Manage end-to-end planning, execution, and governance of regulatory information, data, and systems initiatives.

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• Develop and maintain project plans, milestones, risks, issues, and dependencies.

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• Coordinate business, regulatory, process, and IT stakeholders to ensure effective project delivery.

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• Support implementation activities involving Veeva, medical device content management, and regulatory information management system integrations.

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• Facilitate decision-making, issue resolution, and escalation management.

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• Ensure alignment between business objectives, regulatory requirements, and technical delivery.

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• Provide leadership and support throughout organizational transition and knowledge transfer activities.

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Desired Experience

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• 8–10 years of project management experience, preferably within regulatory affairs and/or the life sciences industry.

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• Experience leading system implementation and business transformation programs.

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• Strong business and technical acumen, with the ability to translate business needs into technology solutions.

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• Proven experience managing cross-functional stakeholders in complex, regulated environments.

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• Familiarity with regulatory information management, Veeva platforms, and related life sciences systems.

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