Director, Oncology Program Management

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General Description

• Lead and/or mentor the program management team for oncology clinical development lifecycle management.
• Develop and lead global product development strategies.
• Establish clear processes for team management and communication.
• Drive strategic team decision-making and delivery of team goals and objectives.
• Lead process improvement initiatives and optimize team efficiency, quality and performance.
• Collaborate with teams to deliver on commitments to the organization and to patients.
  
  

Essential Functions Of The Job

• Plan and execute projects in accordance with the global clinical development strategy.
• Facilitate alignment with key stakeholders and ensure communication across project teams.
• Develop, validate, and maintain project schedules within the enterprise project system.
• Plan, track, and manage project milestones, dependencies, and critical path.
• Lead and facilitate team planning sessions: develop team charter, define project scope, and ensure global cross-functional alignment.
• Implement good project and risk management practices.
• Manage process for project budget governance and oversight within oncology.
• Liaise with internal and external collaborators to deliver high quality work product, presentations, etc.
• Provide internal project management support to core and sub teams, as necessary.
• Coordinate team meeting schedules, prepare agendas and minutes, track action items and progress reports according to project management best practices.
• Lead process improvement initiatives, e.g., budget change control, program management dashboards and reports, risk management, etc.
• Assume additional responsibilities and leadership that are commensurate with experience and expertise such as independently providing alliance management for drug development partners, independently leading oversight steering committees.
  
  

Education Required

• BA/BS degree is required; MA/MS/MBA is preferred.
  
  

Required Experience

• Bachelor's degree with 10 years' of overall experience, 8 years' experience in drug development or commercial within academia, consulting, pharmaceutical or biotechnology industry.
• Master's Degree with 7 years' of overall experience, 6 years' experience in drug development or commercial within academia, consulting, pharmaceutical or biotechnology industry.
• 3 years in leadership roles as leader in a multicultural & international (global) portfolio environment is a plus
  
  

Supervisory Responsibilities

• TBD
  
  

Computer Skills

• Efficient in Microsoft Word, Excel, Project, and Outlook
  
  

Other Qualifications

• PMP certification a plus
  
  

Travel

• As Needed
  
  

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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