Job Information
BeiGene Director, Oncology Program Management in San Mateo, California
Company Overview:
BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. With a team of over 10,000 employees across China, the United States (Cambridge, MA; Ridgefield Park, NJ; Emeryville, CA & San Mateo, CA), Switzerland and Australia, BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer. BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients
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
Minimum Requirements – Education and Experience:
Bachelor’s Degree with 10 + years’ experience in clinical and drug development in the biotech/pharmaceutical industry OR
Master’s Degree or above with 7 + years’ experience in clinical and drug development in the biotech/pharmaceutical industry
5 + years in leadership roles as leader in a multicultural & international (global) portfolio environment is a plus
Other Qualifications:
PMP certification a plus
Supervisory Responsibilities:
Lead and/or mentor program management team
Computer Skills:
Efficient in Microsoft Word, Excel, Project, and Outlook
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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