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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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(min. 10 years experience preferred) Master's degree or Ph.D. in Chemistry, Material Science or similar with focus on construction materials (dry mix mortars and/or water-based products) Fluent English
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accountable for cross-functional work in multiple operational areas including research, laboratory, and production related to probiotic manufacturing activities Duties and Responsibilities: · Has primary
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recommendations Demonstrated ability to manage vendors to ensure effective project delivery Nice-to-Have Master's degree Experience in quality control and/or quality assurance within the pharmaceutical industry
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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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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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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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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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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