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Director, Program Management

Company: Arrowhead Pharmaceuticals, Inc.
Location: Pasadena
Posted on: May 5, 2020

Job Description:

Lead development planning for one or multiple disease area(s) containing a portfolio of early and/or later-stage therapeutic assets.-- S/He will be the point person for Sr. Management regarding the planning, execution, timing, and risk assessment for assigned programs and will be part of the management team to help define and develop organizational level processes. Mentor Senior Program Managers and Program Managers on company processes and help impart skills to allow (SPMs/PMs) to advance to higher levels of responsibility.-- Supervise SPMs/PMs as directed by management.ResponsibilitiesManage a portfolio of therapeutic assets from preclinical to late stage clinicalDrive decision making and issue resolution- identifies bottlenecks including those related to timing, resources and funding, and proactively drives resolution through contingency plans to prevent delays in program milestones.-- When required, step in to fill open gaps to keep programs moving forward effectivelyCollaborate closely with the discovery, clinical, regulatory, commercial, CMC and toxicology team members and senior management, plus external partners to develop and maintain integrated program plans/timelines for the company programs including key commitments, deliverables, resources, and thereby ensuring projects are moving effectively toward their milestones and company goalsInteract effectively with other program managers and their teams to integrate timelines into a unified project/company timeline, identify and resolve crucial bottlenecksTrack progress against program plans, generate regular status updates, and communicate progress and issues to managementActs as an internal spokesperson for the projects in the portfolioIdentifies and resolves conflicts at functional team levelSupervise one or more Program Managers and/or Program AnalystRequirements:College--degree--in biopharmaceutical-related areaA track record in Program Management with preIND through proof-of-concept or late-stage developmentExperience in one or more drug development functions, such as CMC, toxicology, drug discovery, assay generation, or clinical operations in a biotechnology or pharmaceutical environmentWorking knowledge of GMP, GLP, and/or GCP regulations, as well as ICH/FDA guidance documents.Excellent communication skills and ability to work with diverse professionals including all the functional areas involved with development of new therapeutics (e.g. toxicology and other IND enabling groups, clinical research, clinical operations, clinical supply, manufacturing, regulatory affairs, medical writing, commercial and more)Highly motivated team player willing to contribute to a growing biotech organizationStrong--MS--Project, Excel, PowerPoint, and Word skills for Program Management--Demonstrated capabilities and proven track record of problem solving during pre-clinical and clinical drug developmentWillingness and ability to travel as neededPreferred:Ph.D. or other equivalent--advanced--degreeExperience in late stage pharmaceutical development through successful NDA in the pharmaceutical or biotech industryExperience in management of programs with outcomes-based pivotal studiesArrowhead provides competitive salaries and an excellent benefit package----All applicants must have authorization to work in the US for a company

Keywords: Arrowhead Pharmaceuticals, Inc., Pasadena , Director, Program Management, Executive , Pasadena, California

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