Senior Director Project Management

Profile

**MEMBERS ONLY**SIGN UP NOW***., Inc. (“Astex”) is committed to the fight against cancer. Astex is developing a proprietary pipeline of novel therapies for the treatment of solid tumors and hematological malignancies and has several products being developed in collaboration with leading pharmaceutical companies. Astex is a member of the Otsuka group of pharmaceutical companies. which also includes Taiho Pharmaceutical and Taiho Oncology. We are looking for an experienced and motivated professional interested in applying their unique skills to our shared mission. Our office is located in Pleasanton, California in the Rosewood Commons campus near the Dublin-Pleasanton BART station.

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The Senior Director, Project Management will be responsible for managing Astex Pharmaceutical’s late-stage clinical drug development projects. This role will collaborate with the Project Team members to define, plan, and schedule activities to satisfy the project objectives, and work effectively within a diverse and global environment.

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Responsibilities:

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• Drive execution of the integrated project plan within the project team environment Track and control project activities, and ensure coordination of activities between all departments Clearly and proactively communicate progress, issues or deviations that may impact the project schedule, timelines, and costs Lead team members to identify critical path activities, resource constraints, risks and conflicts that may impact the project schedule, timelines, and costs Facilitate and lead effective project team meetings including the creation of effective meeting agendas and clear documentation of meeting discussion points and decisions Maintain and communicate a current overview of project status and issues Assist in budget development and tracking Maintain online project documentation
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Qualifications:

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• Bachelor’s degree or equivalent (scientific or healthcare discipline preferred) Advanced degree and/or PMP certification desirable; PMI certification is a plus Minimum 10 years’ experience in pharmaceutical drug development, preferably oncology Minimum 5 years’ experience managing Phase 2 and 3 stage drug development projects and cross-functional project teams Demonstrated management of a large, global, Phase 3 program Experience managing international teams is desirable Highly motivated with the ability to respond quickly and effectively to a changing environment, and adept at influencing others without direct authority Exceptional planning and organizational skills combined with a broad understanding of late-stage drug development Experience with planning and oversight of project budgets Proficiency with Microsoft Word, Excel, Project, PowerPoint, and Visio
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rn,datePosted:2022-03-02T13:58:00 00:00,validThrough:2022-04-02T03:59:00 00:00,employmentType:FULL_TIME,hiringOrganization:{name:**MEMBERS ONLY**SIGN UP NOW***., Inc. ,@id:248657,url:****California,address:{addressCountry:US,addressLocality:California,addressRegion:California,postalCode:94588,@type:PostalAddress},@type:place},industry:Clinical, Clinical Development, Clinical Project Management, Science/R&D, Oncology,workHours:Full time,educationRequirements:Bachelors Degree,@type:JobPosting,@context:****

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