Director, Oncology Program Management

October 11

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501 - 1000

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. • 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.

Requirements

• 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. • PMP certification a plus.

Benefits

• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness