Director Of Project Management (R&D)

in Healthcare + Life Sciences
  • Massachusetts View on Map
  • Salary: $210,000.00 - $240,000.00
Permanent

Job Detail

  • Experience Level Director
  • Degree Type Bachelor of Arts (BA)
  • Employment Full Time
  • Working Type Hybrid
  • Job Reference 0000017630
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    Lead transformative pharmaceutical projects in a hybrid work setting. Drive impactful lifecycle management and regulatory submission initiatives. Advance your expertise in risk management and operational excellence.

Job Description

Overview

  • Lead strategic program management for late-stage pharmaceutical development and lifecycle projects, ensuring alignment with organizational goals and regulatory requirements.
  • Collaborate across multidisciplinary teams to drive operational excellence and innovative problem-solving approaches in drug development.
  • Oversee program budgets, timelines, and resources, ensuring efficient execution and delivery of project milestones.
  • Enhance program management systems and processes to support organizational growth and adaptability.
  • Facilitate risk management strategies and proactive solutions to address project challenges effectively.
  • Support regulatory submission preparation and execution, ensuring compliance and thorough documentation.
  • Contribute to cross-functional prioritization and decision-making processes to optimize project outcomes.
  • Foster a culture of collaboration, innovation, and continuous improvement within program teams.

Key Responsibilities & Duties

  • Develop and implement integrated program strategies and operational plans for pharmaceutical development projects.
  • Identify and address cross-functional gaps, optimizing execution and resource allocation.
  • Proactively manage project execution, maintaining comprehensive risk management plans and mitigation strategies.
  • Provide leadership and guidance to product teams and sub-teams, ensuring alignment and effective collaboration.
  • Ensure robust communication and logistical operations across the organization to support project success.
  • Contribute to the enhancement and innovation of program management systems and tools.
  • Facilitate transparency and solution-oriented approaches within project teams to drive results.
  • Support regulatory submission processes and lifecycle management planning for investigational drug products.

Job Requirements

  • Bachelor's degree in scientific or engineering disciplines; advanced degree preferred.
  • 12+ years of experience in pharmaceutical product development, including late-stage development and regulatory submissions.
  • Proficiency in MS Project, MS Excel; familiarity with Planview and SmartSheet advantageous.
  • Strong communication, organizational, and time management skills to lead cross-functional teams effectively.
  • Experience in lifecycle management, strategic planning, and risk management within pharmaceutical projects.
  • Ability to work effectively in a matrixed leadership environment, driving collaboration and results.
  • Demonstrated expertise in managing budgets, timelines, and resources efficiently.
  • Commitment to fostering innovation and continuous improvement in program management practices.
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