Associate Director, Project Management

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About the role

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.   Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.   We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description   We are seeking an Associate Director, Global Program Management who will be based in Foster City, CA (hybrid, minimal 3 days onsite).   Job Responsibilities • In partnership with project leaders contributes to the development, approval, and execution the project strategy. • Co-chairs timely, efficient, and action-oriented team meetings and is responsible for coordinating team operations, communications and verifying the timely achievement of deliverables.  Ensures that meeting agendas, materials and minutes are drafted, vetted and shared in a timely manner. • Directs moderately complex project communications and ensures that stakeholders are informed of project activities and their status. • Manages project data in enterprise planning tool, Planisware and partners with other project managers to align and validate data. • Organizes preparation of high-quality documents for review by governance committees in collaboration with the project team and represents the team at Governance meetings, as required. • Facilitates the design, implementation, and life cycle development plan updates. • Provide leadership to the team to anticipate and identify project risks which pose a challenge to achieving strategic goals; proposes and implements plans to mitigate risks or develop contingencies. • Provides project documents and information for monthly reports, quarterly budget reviews, quarterly investor relations/Board updates. • Can facilitate the formation of early-stage development teams with functional area leadership and guide transition of projects between development phases. • Support departmental continuous improvement and optimization initiatives. • Ensures project work complies with established practices, policies and processes.   Basic qualifications: Bachelor's Degree and Ten Years' Experience OR Masters' Degree and Eight Years' Experience OR PhD/PharmD and Five Years' Experience   Preferred Qualifications:   • Experience to include 5+ years of leading cross-functional project management activities within the pharmaceutical and related industry, building, managing, and articulating comprehensive, complex, cross-functional plans. • PMP (Project Management Professional) or other PM certification, or equivalent a plus. • Strong knowledge of the drug development process and comprehensive understanding of and application of principles, concepts, practices, and standards of pharmaceutical project management. • Expertise in developing and managing project scope, deliverables, risks and resource requirements. • Leadership presence with the ability to translate strategy into action

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