Job Description
**_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.
**Education Required:**
+ BA/BS degree is required; MA/MS/MBA is preferred.
**Required Experience:**
+ Bachelor's degree with 8 + years' overall experience in drug development or commercial within academia, consulting, pharmaceutical or biotechnology industry.
+ Master's Degree with 6 + 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.
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