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resources to ensure all functional device activities are completed on schedule following the Pfizer Design Control process. Utilize technical writing and statistical data analysis skills to write protocols
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve As a Senior Associate Scientist, you will be
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, HTRF, TR-FRET, SPA, luminescence, flow cytometry, high content imaging) commonly used in pharmacology screening PHYSICAL/MENTAL REQUIREMENTS Lifting, sitting, standing, walking, bending Ability
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notifying instrument key operators of upcoming reagent/supply needs. Process samples for analysis or storage. Utilize PIMS/LIS computer system for the processing of samples. Collect biological samples from
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relevant inbound queries from HCPs via established triage process. In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical (WRD) and Global Product
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triage process. In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical (WRD) and Global Product Development (GPD) in the identification
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triage process. In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical (WRD) and Global Product Development (GPD) in the identification
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, organizing analytical processes and workflows, and mentoring/developing the managers what work on your team as well as junior team members. Drive the delivery process, leveraging agile methodologies and best
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high impact project opportunities and process changes. Use advanced machine learning techniques for driving highly applied analyses and tools to directly drive revenue and optimize resources. BASIC
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve You will participate in pre-clinical oncology