1,339 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"MPG" positions at Stony Brook University
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without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all
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without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all
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without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all
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without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all
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, disability, genetic information, veteran status and all other protected classes under federal or state laws. If you need a disability-related accommodation, please call the university Office of Equity and
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. Experience in environmental quality, limnology, Biology, Marine Biology and/or environmental protection programs. Experience with organizing and analyzing large data sets. Experience in writing reports
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education and/or administrative experience totaling four (4) years may be considered. One (1) year of full-time administrative experience in a healthcare setting. Ability to utilize various computer programs
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preclinical or translational data into IIT protocols to enhance scientific justification and translational relevance. ● Maintain consistency in language, structure, and format across IIT protocol templates
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are not limited to: • Collects data through observation and communicates information to assist the RN and/or provider in patient assessment and care planning. • Participates as a member of the health care
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of Principal Investigator/Cancer Clinical Trials Administrative Director. Includes screening, eligibility, data collection, adverse event reporting, completion of CRF's and all regulatory requirements per