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Director, Oncology Program Management

San Mateo, CA, United States

**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:**

**Bachelors Degree with 10 + years experience in clinical and drug development in the** **biotech/pharmaceutical** **industry** **OR**

**Masters 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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