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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
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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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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 to Apply for Job: April 19th, 2024
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work in a GMP environment. Comprehensive knowledge of analytical techniques in Chemistry, Bioanalytical, or Microbiology. Relevant pharmaceutical experience. Nice-to-Have Master ' s degree in
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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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/verification protocols Supervision and direction of others performing this work Perform routine periodic review activities Provide/maintain Site Validation Master Plan information Support regulatory audits
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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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(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