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the lifecycle of original research projects from abstract to publication. Assists with the production of images and presentation materials to specification. Organizes original research abstract submission
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the conduct of the study to enable quality, compliance and patient safety at the trial, site and patient level. Interacts with DMCs and steering committees as required. Is responsible for ensuring all materials
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to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and
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