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Global Asset Lead

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Jobtailor
Full Time position
Listed on 2026-08-16
Job specializations:
  • Management
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 180000 - 240000 USD Yearly USD 180000.00 240000.00 YEAR
Job Description & How to Apply Below
  • Lead the cross-functional Global Asset Team and build the vision and strategy to maximize asset value
  • Create scientific and commercial value from early development through commercialization and patent expiry
  • Own the overall program strategy, establish project goals, and lead cross-functional teams
  • Define integrated development strategies and executable high-level roadmaps
  • Oversee operations, align functions, and drive operational excellence
  • Evaluate medical literature and competitive developments to inform lifecycle management strategy
  • Set product strategy and operational priorities aligned with corporate objectives
  • Drive development, registration, launch, market-facing activities, and lifecycle management initiatives
  • Lead communications with internal and external stakeholders
  • Report progress, risks, and opportunities to functional and executive leadership
  • Represent the asset in Ipsen Governance Committees
  • Serve as ambassador for the asset and Ipsen across scientific, healthcare, patient, and partner communities
  • Define resource requirements and challenge resource allocation decisions
  • Develop and execute comprehensive risk mitigation plans
  • Build and lead high-performing cross-functional teams
  • Mobilize resources across a complex global matrix through influence and collaboration
  • Foster innovation, agility, and continuous improvement
  • Ensure compliance with R&D SOPs, GCP standards, applicable regulations, and Ipsen policies
Requirements
  • Advanced degree in Medical or Life Sciences, such as MD, PhD and/or MBA
  • Board certification in Oncology or Hematology highly valued for physician candidates
  • Minimum 5 years of global project leadership experience within biotechnology or pharmaceutical environments
  • Demonstrated success leading complex global matrix teams and influencing without formal authority
  • Experience across Clinical Development, Clinical Operations, Commercial, Market Access, Regulatory, Safety, Medical Affairs, and Project Management
  • Deep understanding of oncology and the competitive landscape
  • Strong external scientific networks highly advantageous
  • Visionary leadership with ability to inspire others and build high-performing teams
  • Ability to balance short- and long-term priorities
  • Ability to navigate complexity and solve critical business challenges
  • Ability to lead with authenticity, courage, and impact
  • Ability to deliver activities in compliance with R&D SOPs, GCP standards, applicable regulations, and Ipsen policies
Core Competencies

Demonstrates expertise in leading cross-functional teams and developing integrated strategies to maximize asset value in the biotechnology or pharmaceutical sectors. Possesses a deep understanding of oncology, regulatory compliance, and the ability to navigate complex global environments while fostering innovation and operational excellence.

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