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Global Project Leader, Metabolic Diseases – Early Portfolio
Novo Nordisk. Lead highly complex metabolic disease product projects with significant business and portfolio impact .
Posted 9/23/2026full-timeBoston • Massachusetts • United StatesSenior💰 $229,200 - $401,100 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in leading complex, cross-functional global development projects within the pharmaceutical value chain, with a strong focus on stakeholder engagement, strategic execution, and compliance with regulatory standards. Proven ability to influence and drive innovation in a matrix organization while aligning project goals with corporate strategy and sustainability commitments.
Highest-signal resume keywords
Project LeadershipCross-Functional CollaborationStakeholder EngagementPortfolio ManagementRegulatory Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project DefinitionRisk ManagementStrategic PlanningExecutionCommunicationGovernance InteractionsLong-Term StrategyPortfolio ManagementClinical Trial SOPsInnovation Mindset
Soft Skills
MentoringInfluencingAccountabilityContinuous ImprovementCollaboration
Industry Keywords
Pharmaceutical Value ChainGlobal Development ProjectsMatrix OrganizationNovo Nordisk WayStakeholder Relations
About the role
Key responsibilities & impact- Lead highly complex metabolic disease product projects with significant business and portfolio impact
- Own the full product development lifecycle, including long-term decisions and implications
- Define, organize, and lead research and development deliverables toward global product approval
- Make prioritizations and trade-offs to maximize value, quality, and long-term impact across markets and customer groups
- Secure senior management and governance-board endorsement by clarifying decision choices, implications, and accountability
- Identify synergies and dependencies across functions and projects to align resources
- Assess project relevance and risks against future market and regulatory needs
- Define project goals and objectives and align with Lines of Business leaders on performance and growth areas
- Coach, mentor, and provide feedback to Global Project Team members
- Foster transparent stakeholder engagement, collaboration, direction, alignment, and accountability across the matrix
- Build and maintain relationships with internal and external stakeholders, opinion leaders, health authorities, investigators, CROs, vendors, and partners
- Communicate and negotiate globally with internal and external stakeholders, including regulatory authorities
- Connect global and local teams and support affiliates in strategic and tactical execution
- Communicate project reality, progress, options, trade-offs, and dilemmas to governance bodies and senior leadership
- Shape project strategy and recommend development options to governance boards
- Apply portfolio, launch, lifecycle, and cross-functional value-chain expertise
- Chair one or more Global Project Teams and lead end-to-end product development across drug, device, digital, data, and diagnostics
- Deliver approved milestones and objectives and report progress, deliverables, milestones, resource use, budgets, and financial targets
- Manage interdependencies across Lines of Business and align with corporate and R&D strategy and sustainability commitments
- Plan, monitor, and continuously improve complex development activities
- Coordinate complex work across functions and external partners, challenging the status quo and driving innovation
- Represent the VP area in relevant internal and external forums
Requirements
What you’ll need- Bachelor's degree from an accredited university and 14+ years of experience required; equivalent advanced-degree pathways include Master's degree and 12+ years, PhD and 10+ years, or MD/DO and 5+ years
- Extensive senior-level experience, typically 12+ years, across several relevant functional areas
- Proven leadership of complex, cross-functional, global development projects in a matrix organization
- Experience across the pharmaceutical value chain within Novo Nordisk and/or other pharmaceutical organizations
- Broad T-profile with leadership responsibility and experience in both project and people leadership
- Ability to influence in a matrix organization
- Role-model behavior aligned with the Novo Nordisk Way, including accountability, continuous improvement, innovation mindset, and enterprise-minded leadership
- Expertise in project definition/initiation, planning, execution, risk management, completion, communication, stakeholder relations, strategy, and affiliate interaction
- Advanced expertise in cross-functional processes and governance interactions, portfolio management, long-term strategy, and translating insights into strategy and tactics
- Ability to travel domestically and internationally
- Ability to work in accordance with Novo Nordisk clinical trial SOPs, applicable policies, PDP, and the Novo Nordisk Way
Benefits
Comp & perks- Company bonus based on individual and company performance
- Long-term incentive compensation and/or company vehicles depending on position level or company factors
- Medical coverage
- Dental coverage
- Vision coverage
- Life insurance
- Disability insurance
- 401(k) savings plan
- Flexible spending accounts
- Employee assistance program
- Tuition reimbursement program
- Group legal insurance
- Critical illness insurance
- Identity theft protection
- Pet insurance
- Auto/home insurance
- Sick time
- Flexible vacation policy
- Parental leave policy