Senior Director, Program Lead

Company DescriptionDeciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines and providing hope to people living with cancer, neurologic and autoimmune disease. Deciphera is leveraging its proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines. In addition to advancing multiple product candidates from Deciphera’s platform in clinical studies, QINLOCK (ripretinib) is Deciphera’s switch-control kinase inhibitor approved in many countries including the European Union and the United States for the treatment of adult patients with advanced gastrointestinal stromal tumor (GIST) who have received prior treatment with 3 or more kinase inhibitors, including imatinib. ROMVIMZA (vimseltinib) is a kinase inhibitor approved in the United States for adult patients with symptomatic tenosynovial giant cell tumor (TGCT) for which surgical resection will potentially cause worsening functional limitation or severe morbidity, and in the European Union for adult patients with TGCT associated with clinically relevant physical function deterioration and in whom surgical options have been exhausted or would induce unacceptable morbidity or disability. The spirit of collaboration that has brought medications to life continues to guide how we operate, grow, and discover new breakthroughs. We cultivate an inclusive culture that values curiosity, creativity, and shared accountability—empowering individuals to challenge the unknown together. Deciphera offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance and a flexible spending account for either health care and/or dependent care.Job DescriptionRole Summary: Deciphera’s cross-functional program teams drive the strategy and operations of our late preclinical, clinical, and commercial assets. We are seeking a dynamic, seasoned Sr Director, Program Lead (PL) who will be responsible and accountable for one or more therapeutic assets. The successful candidate will be a strategic leader who can leverage their strong drug development expertise, EQ, and organizational skills to develop and drive the asset strategy and for leading all development and life-cycle management projects associated with the asset. Key attributes of the successful candidate include:Key Responsibilities:Program Strategy & Execution Accountability (60%)For a given asset/program, responsible for the development and execution of the overarching global program strategy. The PL leads all research and development activities associated with an asset from approximately nomination of lead candidates to the marketplace with full accountability.Drive the development and execution of the strategic plan, appropriately balancing data quality, timelines and costs based on current internal corporate considerations and the external landscape.Lead one or more cross-functional program teams to define program vision, strategy, goals, decision points, investments and areas of risk and associated mitigations and contingencies.Partners closely with the program manager to provide strategic, process and operational leadership to the Program teamIdentifies and communicates risks and appropriate mitigationsLead data-driven decision-making processes to enable timely and objective development decisionsCommunicate (20%)Holistic and confident communication: ensure PT clearly understands expectations from leadership, ensure leadership clearly understands program status, timelines, milestones, risks and mitigationsFocus team efforts on most critical tasks; identify and resolve communication bottlenecksParticipate in Portfolio Strategy Steering Committee meetings as the key representative of the program teamLiaise with relevant stakeholders within the Ono Pharma Group to ensure alignment across entities. Liaise with peers within the Program Leadership and Management function to maintain consistent cross-project standards, ensure aligned strategies, and to determine overlap of competing priorities.Promotes organizational reputation by engaging with internal and external stakeholders and collaborating actively with other Deciphera PLs (20%)PLs are experienced, versatile and strong enterprise leadersPLs are highly collaborative cross-functional leaders who consistently drive top performance and deliver against challenging goalsPLs ensure that risks and challenges are addressed proactively and collaboratively with partner functions, with joint decision making when appropriate to drive, deliver and maximize asset value.PLs are effective in communicating to partners and stakeholders at an appropriate level of detail.Other duties and responsibilities as assigned.QualificationsA minimum of 15 years drug development experience in the biopharmaceutical industry including a minimum of 3 years’ development program leadership experienceSolid understanding of drug development process (steps, functions and their roles, key interdependencies)Strong interpersonal skills, with a proven track record of influencing without authority across a matrixed organizationHighly effective influencer without authority at all levelsBuilds consensus, but identifies a final decision maker / escalates when requiredOutstanding written and oral communicator, able to clearly and accurately express complex ideasDemonstrated ability to be flexible and open to adjusting approaches as new information or circumstances emergeResilient in a fast-paced, rapidly evolving environmentHighly motivated with a "hands on" leadership style - no task is too big or small!Strategic, efficient, organized, and empathetic leader who can zoom both in and outCommitted to driving the program forward to the next strategic inflection point to enable an informed decision for next steps, in line with corporate objectives.Preferred CapabilitiesHas experience managing cross functional teamsLate Phase/commercial experience a plusExperience working with the Alliance and Business Development Teams and understanding the importance of partnershipsExperience with MS office suite (PowerPoint, Excel, MS Teams) required, project management tools (Smartsheet, ThinkCell, MS Project) a plusAdditional InformationDeciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $226,200 - $310,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.​Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)EQUAL EMPLOYMENT OPPORTUNITY INFORMATIONDeciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.SummaryType: Full-timeFunction: ScienceExperience level: Mid-Senior LevelIndustry: Pharmaceuticals