**_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. **Required Experience:** + Bachelor’s degree with 10 + years’ overall experience in drug development or commercial within academia, consulting, pharmaceutical or biotechnology industry. + Master’s Degree with 7 + years’ overall 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.