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.
Director Of Project Management (R&D)
in Healthcare + Life Sciences PermanentJob Detail
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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