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of bodily fluids. Ability to lift racks/boxes up to 10 lbs NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS This position might require occasional weekend work to meet critical timelines Other
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development strategy and program execution of research projects with a particular focus on obesity and associated conditions (e.g., cardiovascular disease, renal impairment, diabetes, etc.), and lead
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for the implementation and execution of initiatives and strategizes creative solutions to complex formulations/programs for internal work as well as work conducted externally at CROs while maintaining a dynamic
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used in the development of Pfizer medicines. A knowledge of pharmaceutical development, analytical measurements, formulation & process development, as well as relevant computational skills are desirable
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ensures successful global program implementation through oversight and review of the global program design including the clinical development plan or lifecycle strategy. The clinician medical monitor
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project/portfolio tracking tools. Responsible for program updates to Senior Management, proactively and in timely manner. Lead introduction and implementation of project management related strategic
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delivery timelines, using project/portfolio tracking tools. Responsible for program updates to Senior Management, proactively and in timely manner. Lead introduction and implementation of project management
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responder hypotheses, elucidate mechanisms of resistance and identify rational drug combinations that can be translated to the clinic Work collaboratively with computational biology group to integrate complex
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to the clinical development plan. Designs clinical studies to meet the stated objectives. Assures that clinical trial objectives fit with the clinical program strategy. Ensure that documents (protocol, Informed
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be translated to the clinic Work collaboratively with computational biology group to integrate complex data sets including 'omic' data in preclinical/non-clinical settings to deepen understanding