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Experience in Engineering or equivalent field of study research including in the peer-reviewed Engineering or equivalent field of study literature and/or the patent literature.
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Particularly noteworthy opportunities for undergraduates include the Charles A. Dana Research Institute for Scientists Emeriti (RISE), the Drew Summer Science Institute (DSSI), the Center for Civic Engagement, as well as seven New York City semesters and several international study abroad programs.
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Our rigorous academic curriculum builds strong foundations in mathematics, science, social studies, English and language arts along with exposure to foreign language study. Through art, nature, literature, dramatic play, language, writing and music, our Reggio-inspired program nurtures students’ innate curiosity, intellect, creativity and self-confidence.
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Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, presentation materials and publications to medical journals.
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Substantial clinical study protocol experience, as lead author, required. Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus. MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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This role will assist in various tasks, including literature review, study design, survey development, quantitative and qualitative data collection and analysis, training program development, manuscripts/reports writing, student supervision, and will work with Dr. Chen for coordinating and managing relevant projects as well as other duties as assigned.
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The College of Humanities and Social Sciences' departments and programs offer students the breadth of a traditional liberal arts education in the humanities and social sciences while preparing them for a wide range of professions, for graduate school, and for advanced professional study in fields such as law, education, public administration, clinical psychology, and business.
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Ascent Classical Academies are dedicated to delivering a content-rich curriculum in the liberal arts and sciences, with underlying principles in the Western tradition of the study of history, literature, philosophy, and fine arts.
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Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.
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Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.
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Presents relevant special topics in professional literature at clinic meetings, grand rounds, conferences, university settings and meetings as delegated or requested by the faculty. Serves as a clinical resource for hospital and/or system or departmental committee/task force or initiates and/or provides leadership in an ongoing departmental interest/study group.
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Toxicology systematic review tasks including literature screening, study quality evaluation, study data extraction, dose-response analysis, incorporation of NAMs and mechanistic data, and data synthesis.
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Project and technical support of activities on multiple projects concurrently involving toxicology data, systematic literature reviews, and risk assessment. Experience with systematic literature review.
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Not required, but experience with orphan drug designations and PSP/PIPs a plus. The ideal candidate would hold a Bachelors, Masters, or Ph. D. in scientific, medical, clinical discipline. Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools.
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