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Teva Associate Director Project Manager 
United States, Pennsylvania, East Bradford Township 
46425470

24.09.2024

The Project Manager has overall responsibility for leading the global development of R&D Innovative Medicine products; ultimately to maximize the product’s potential. The PM may work in partnership with a more Senior Project Leader to establish, maintain and deliver the priority product plan for both early and late stage. Will also lead established projects alone and based on experience and expertise early stage programs as well. Responsible for delivering a product development strategy approved by governance and securing investment for the development program

How you’ll spend your day
  • Lead the cross-functional project team to secure approval and funding for the overall product development plan and through the strategic planning and delivery of the development program, proactively identifying and managing issues and risks and ensuring decisions are made at the appropriate levels and with the appropriate cross-functional input.
  • Lead cross-functional delivery to the agreed development budget and timeline – collaborating with the cross-functional team members to track and manage issues in budget and timelines and bringing significant variations to R&D management for approval based on agreed trashold
  • Collaborate with function leads to ensure their teams are fully resourced and skilled appropriately to deliver, working expeditiously to highlight any resource gaps that impact the program delivery or quality. Participate in sub-team leadership.
  • Lead quality risk management to ensure significant risks to the programs have planned mitigations and are flagged in terms of likelihood and impact, to the relevant leadership.
  • Develop and manage end to end product development plans in Planisware to accurately reflect the tactical plan/timeline and interrelated functional.
  • Ensure all relevant documentation is accurate, current, and approved by respective leadership.
  • Manage multiple projects, programs or a large portfolio of inter-related projects
  • Willingness and ability to routinely travel domestically and abroad.
Your experience and qualifications

Requirements:

  • Master’s level degree in life scientific field
  • Minimum 5 years of experience in the pharmaceutical industry
  • Established track record of effective and influential oral presentations
  • Understanding of innovative drug development, industry guidelines, and regulatory and submissions processes globally

Preferred:

  • Advanced scientific degree (M.D., D.O., Ph.D.)
  • Advanced experience leading a cross-functional project teams

Specialized or Technical Knowledge:

  • Project Management Professional (PMP®) preferred
  • Excellent computer software skills, specifically – Planisware / Microsoft Project, SharePoint, PowerPoint, Word, Excel and Outlook
  • In-depth knowledge of the innovative drug development process

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