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POSITION SUMMARY You will join a team of scientists supporting oncology development programs. You will be the primary Clinical Pharmacology Lead providing clinical pharmacology expertise to a
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collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Bachelors required and 15+ years' experience; Masters
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JOB SUMMARY The Site Care Partner is the main Pfizer point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety at the investigator site
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Role Summary The Site Care Partner is the main Pfizer point of contact for investigative sites, responsible for building and retaining relationships from site activation through the lifecycle
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documentation systems Nice-to-Have Master's degree Experience engaging in the external regulatory and pharmaceutical environment 2+ years of hands-on CMC authoring experience (investigational, initial
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projects to expand and maintain the system. Collaborating with the Infrastructure lead on strategy, methodologies, master planning and documentation of the PI data historian to align with industry best
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Will Achieve It Responsibilities include the following: Leading process validation activities: Defining PV strategies in a process validation master plan Generating protocols, evaluating data, and
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regulations Understand and can challenge scientific arguments, identifies regulatory scientific data needs and solves regulatory issues. Serve as primary contact to FDA (or other relevant regulatory authorities
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, & PowerPoint PREFERRED QUALIFICATIONS MBA or master's level education Previous experience in managed markets analytics or a job function supporting the promotion of pharmaceuticals. Other Job Details: Last Date
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working to the overall plan, including management of and reporting. Support development of the Site Master Plan and Site Space Plan to ensure effective and strategic use of assets and capital investment