... function and cross-functionally with other departments. Responsibilities for this position include: Lead ... investigational Exelixis product(s). Lead the cross-functional Benefit Risk Team for the assigned Exelixis ...

... development process from generation of the master label text to label printing. Lead the development, review and User Acceptance Testing (UAT) of the Interactive Response Technology (IRT) system. Co-lead the ...

... Reference #: JR5716 SUMMARY/JOB PURPOSE: Responsible for primary regulatory review of promotional m ...

... Reference #: JR5673 SUMMARY/JOB PURPOSE: In collaboration with the Exelixis clinical teams, the Sen ...

... Reference #: JR5223 SUMMARY/JOB PURPOSE: In collaboration with the Exelixis clinical teams, the primary role is to lead and execute early/late stage clinical trials for oncology products in development ...

... depots and clinical sites. Essential Duties And Responsibilities: Lead effort for clinical supply ...

... analyses, such as Integrated Safety Summaries. * As the lead or support programmer on studies, work with ... delivery of required outputs * As the lead programmer, responsible for helping to identify when additional ...

... intelligence to assess the impact on Exelixis and advise Regulatory Affairs leadership accordingly. Lead ...

... Reference #: JR5691 SUMMARY/JOB PURPOSE: Manage and perform the operational activities around regula ...

... partners, and support Data Managers, may serve as the lead study data manager for a large, complex trial or ... deliverables with quality and per agreed timelines * Lead the planning and execution of data management ...

... : Lead and oversee development plans incorporating regulatory strategies designed to maximize chances of ...

... . Supervisory Responsibilities: Co-Lead across functions within Medical Affairs to support projects No direct ...