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withstanding regulatory scrutiny. This position will focus primarily in Trial Master File Operations. Facilitate the execution of the TMF Operations' activities to enable complete, compliant and consistent study
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first in human (FIH) through proof of concept (PoC) studies, including proof of mechanism (PoM) and early signals of efficacy (ESoE) studies in a given therapeutic area. The primary therapeutic areas
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andtherapeuticsin all indications ensuring alignment among the overall strategic, operational, and line plans. Interact closely with scientific staff to understand everyday facility challenges. Manage vaccine
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with 8 years of experience OR a bachelors with at least 5 years of experience OR Masters Degree with more than 3 years of experience, OR a PhD with 0+ years of experience. 5+ years of demonstrated
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making analytics and ensure that assigned initiatives are in alignment to Pfizer SAS SOP's and Policies. The individual will primarily be aligned to the Specialty Pharmacy Centers of Excellence, but may
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interpersonal and communication skills Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives Proficiency with computer applications (MS Office) Nice-to-Have Master's degree
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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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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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JOB SUMMARY The Site Care Partner is the main Pfizer point of contact for investigative sites throughout a study life cycle; accountable for site start-up activities through activation; accountable
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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