Pay range : $48 / hr to $53 / hr
Job Description : Location : Seattle-Dexter, WA
Top Skills :
Experience in the Biotech / Cell Therapy industry PreferredPMP Experience PreferredExperience with Smartsheets, Tableau, and MS ProjectsStrong organizational skills, ability to multi-task and work in a dynamic, fast paced environment.The Project Manager is closely partnered with the Client&T Leader to enable effective execution of strategy and plans. The scope of responsibilities of the Project Manager fall into 4 general categories which flex across all drug modalities, disease areas and stages of development.
1. Cross-functional Project Management to ensure integrated execution of LCM strategy and communication
2. Project Timeline Management and timeline scenario planning
3. Assist with Gaps Analysis and Risks Management
4. Ensure connectivity with key partners on critical actions, timelines etc
Primary Responsibilities :
In partnership with Client&T Team Leader, manage multiple commercial LCM program assignments (actual number determined by level of project complexity and candidate experience) and drive execution of integrated program strategyDevelop detailed project plan that is aligned with the overall strategy. Work collaboratively with the CTO team leaders and cross functional teams to track all project milestonesFacilitate pertinent scenario planning to address changing business / clinic needs. Gather stakeholder input, evaluate, collate, manage and communicate implications and adjustments to the overall planManage all meeting logistics including the creation of clear, concise minutesPartner with the GM&ST Leader to facilitate the management and communication of program risks and mitigation strategiesLeverage portfolio and program management tools to track program execution, milestones, risks, and long range planning to ensure appropriate communication to team members and management. Examples include MS Project Server, ePlan, PSI CMC database, OnePager Pro, DOI Tool, Right First Time Scorecard, Operational Risk ManagementCoordinate and ensure appropriate allocation of DS and API materials for non-clinical useExperience / Qualifications :
Bachelor's degree in engineering or relevant scientific discipline with at least 5 years of relevant experience / Masters' degree with a minimum of 2-6 years of relevant experienceHighly motivated self-starter that works well both in teams as well as independentlyStrong project management, business process management, and optimization skillsFamiliarity with end-to-end CMC drug development with an understanding of critical milestones and typical bottlenecks preferredStrong organizational skills, ability to multi-task and work in a dynamic, fast paced environment.Demonstrated ability to accomplish results and meet deadlines and commitmentsStrong interpersonal and communications skills, both oral a writtenDemonstrated proficiency in MS Project, PowerPoint, Excel and WordDemonstrated ability to build relationships, influence, negotiate, and drive organizational engagementExperience developing and / or managing program management tools to forecast budgets, timelines and resources preferredPMP Preferred
Salary : $48 - $53
