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.