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Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Director Project Management

Program ManagementConfirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listedIn-person

About the Job

Requirements

  • A Bachelor of Science degree in Life Sciences and at least 8 years of experience in the biotech or pharmaceutical industry, including at least 5 years of direct development project management experience managing cross-functional global development teams.
  • Broad knowledge of the clinical drug development process, regulations, and launch preparation, with strong proficiency in project management practices, tools, and methodology.
  • Expertise in developing and managing project scope, deliverables, risk and resource requirements, schedule and timeline management, and risk management.
  • Clear, succinct, and timely communication and the ability to foster important relationships with key stakeholders.
  • Outstanding verbal and written communication skills, including the ability to summarize complex information simply and interact effectively across team functions and with external key stakeholders.
  • A proven track record of sound decision-making and judgment.
  • Experience using project management software to manage project timelines and resources, such as MS Project, SmartSheet, OfficeTimeline, and OnePager Pro.
  • Strong computer proficiency with the MS Office suite, SharePoint, and similar document archiving systems.

Responsibilities

  • Partner with functional leaders in Japan to define project strategy, manage stakeholders, and address overall project leadership topics.
  • Establish and maintain a functionally integrated project plan and project assumptions, accounting for goals, key objectives, deliverables, and risks, to support accurate project, financial, and portfolio analyses for planning processes.
  • Ensure project risks are identified and managed, working with subject matter experts to construct appropriate mitigation plans.
  • Lead monitoring and tracking of project progress and evaluate alternative project scenarios, including costs, timelines, risks, and project strategy, as the program progresses through stage gates and as business needs require.
  • Lead efficient information flow to the global cross-functional project team and internal advisory and governance bodies.
  • Manage meetings and information effectively by prioritizing discussion topics, ensuring meeting objectives are achieved, communicating decisions to key stakeholders, and ensuring action items are assigned and completed in a timely manner.
  • Own project team information, including the project plan, budget, and program assumptions, as approved by local governance and the Senior Leadership Team.
  • Apply drug development and commercialization expertise to coach and mentor project team members to support efficient and effective team operation.
  • Identify, recommend, and implement opportunities to streamline team and business processes.
  • Participate in establishing and implementing project management systems and best practices.
  • Coach and mentor Project Management team members to build a strong bench of future leaders.

Desired Qualifications

  • An MSc., MBA, or Ph.D. in Life Sciences.
  • PMP (Project Management Professional), another project management certification, or equivalent.
  • Experience in the oncology therapeutic area.

About the Company

Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Revolution Medicines develops precision oncology drugs focused on cancers driven by RAS mutations. Its RAS(ON) inhibitors are small molecules that bind the active form of RAS to block cancer signaling, with candidates like Daraxonrasib (RMC-6236), Elironrasib (RMC-6291), and Zoldonrasib (RMC-9805) advancing in global Phase 3 trials. The company funds its research through collaborations, royalties, and upfront funding, and has not yet marketed a product. Its goal is to bring effective RAS-targeted therapies to patients and advance multiple candidates through late-stage trials toward approval, supported by strong cash reserves.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Redwood City, CA
Founded
2014

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