Associate Director, Program Management

Associate Director, Program ManagementFoster CityMissionMirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we're looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.Position SummaryThe Associate Director, Program Management plays a central role within Mirum by providing program management expertise and ensuring cross-functional planning and execution. The program manager partners with the Program Lead and functional leads to develop and manage the integrated product plan, develop timelines, and ensure adherence to the budget for one of our pipeline programs.Job Functions/ResponsibilitiesSupport the Program Lead with the development, communication, and timely execution of the program strategyOrganize and drive effective and action-oriented program team meetings by preparing and distributing agendas/minutes, identifying and tracking decisions and action items to resolution, and escalating areas of concern as neededPartner with the Program Lead to facilitate effective cross-functional decision making with transparent communication and clear escalation pathwaysFacilitate identification of risks which could impact the program's strategic goals; propose and implement plans to mitigate risks or develop contingenciesDevelop and maintain integrated program timelines in conjunction with functional leadsIdentify and communicate program priorities, interdependencies, and critical path activities to all stakeholders to allow long term planning, including resource allocationOrganize the preparation of high-quality documents for review by governance committees in collaboration with the Program Lead and program teamPrepares and provides project documents and information for monthly reports, executive team updates, and board meetings.Partner with Program Lead and finance and accounting to develop annual operating plan components related to assigned program and support budget management by timely identification of out-of-scope activitiesCoordinate and manage special program-related projects, as assignedContribute to the standardization of project management best practices at MirumQualificationsEducation /Experience:Bachelors Degree or higher in scientific/healthcare/business fieldExperience (7+ years) in clinical research and project management within the pharmaceutical industry (Biotech/small pharma experience preferred).Experience in rare disease and/or liver disease is a plus.Knowledge, Skills and Abilities:Strong ability to communicate effectively with team members creating an environment that fosters successful teamwork, collaboration and cooperation.Thorough understanding of clinical trial management processes and the operation of all clinical development functional areas.Demonstrated ability to prepare timelines and present related information to management.Proven ability to identify risks, propose mitigation strategies, and remove barriers to success.Strong attention to detail and the ability to work collaboratively with Project Lead to establish priorities for team.Expertise in developing and managing project scope, deliverables, risks and resource requirements.Strong knowledge of project management software packages and the Microsoft Office Suite: Excel, Project, PowerPoint, Word and Outlook; ability to create effective presentations for internal and external use.Ability to work in a fast paced environment with demonstrated ability to juggle multiple competing tasks and demands, across time-zones, while maintaining positive attitude.Ability to work independently, take initiative, complete tasks to deadlines and support product team in doing the same.Excellent written and oral communication skills.Displays a high level of professionalism with internal and external stakeholders.Knowledge of current regulatory requirements and guidelines governing clinical research. (e.g. ICH/GCP).The salary range for this position is $195,084 to $225,217 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee's geographic location.