
Director, Pharmaceutical/Biotechnology Program Management
Emeryville, CAJobSeen 1mo agoSeen in employer's feed 4 days ago
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
Leads program management for oncology drug development, partners with the team lead to develop global strategies, establishes clear processes, drives strategic decision‑making, improves team efficiency and performance, collaborates to meet commitments to the organization and patients, plans and executes projects, facilitates alignment with stakeholders, maintains integrated project plans, provides visual project plans, manages milestones, budgets, risks, and coordinates meetings while assuming additional leadership responsibilities.
Skills & qualifications
Skills
Qualifications
Full job description
General Description:
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Lead program management for oncology drug development and product lifecycle management.
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Partner with Team Lead to lead development of global product development strategies.
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Establish clear processes for program team management and communication.
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Drive strategic team decision-making and delivery of team goals and objectives.
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Lead process improvement initiatives and optimize team efficiency, quality and performance.
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Collaborate with team to deliver on commitments to the organization and to patients.
Essential Functions of the job:
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Plan and execute projects in accordance with the global asset development strategy.
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Facilitate alignment with key functions and stakeholders and ensure communication across project team.
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Develop, validate, and maintain integrated project plan(s) within the enterprise project system.
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Provide visuals of project plans for use with teams and other stakeholders.
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Ensure team understanding, alignment and achievement of key goals, milestones and deliverables.
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Plan, track, and manage project milestones, dependencies, and critical path.
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Facilitate team planning sessions: develop team charter, define project scope, and ensure global cross-functional alignment.
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Implement good project and risk management practices.
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Manage process for project budget oversight, planning and control.
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Liaise with internal collaborators to deliver high quality work product, presentations, governance investments and updates etc.
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Provide internal project management support to core and sub teams, as necessary.
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Coordinate team meeting schedules, prepare agendas and minutes, track action items and progress reports according to project management best practices.
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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 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
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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