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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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reports. Motivate personnel by setting high standards, encourage teamwork. Clear, unambiguous communication is critical. Primary contact for all personnel issues occurring within the department. Responsible
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Bachelor's with at least 5 years of experience. OR Master's Degree with more than 3 years of experience. OR a PhD with 0+ years of experience. Experience with writing software test plans, user requirements
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of project planning and resource forecasting tools and systems (e.g. Microsoft Project, Planisware)) Rapidly mastering new software tools Nice-to-Have Project Management for Professionals (PMP) Certification
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directly impact patients. What You Will Achieve The primary responsibility of this position is to provide logistical support to clinical study teams for Vaccine Research and Development (VRD) clinical and
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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
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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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-to-Have Master's degree Experience engaging in the external regulatory and pharmaceutical environment 2+ years of hands-on CMC authoring experience (investigational, initial registrations or post-approval
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degree with eight years of experience; OR a Bachelor's degree with at least five years of experience; OR A Master's degree with more than three years of experience; OR a Ph.D. with 0-2 years of experience
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ROLE SUMMARY Summarize the primary purpose & key accountabilities of the role, including geographical scope (i.e. Global vs. Country/Region). Summary should be concise and include strategic