663 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UNIV" "Univ" "UNIV" uni jobs at University of Pennsylvania
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manufacturing data:, and annual reporting to regulatory bodies, and any FDA requests for information. The Manager of the Regulatory and CMC unit is a supervisory role and will direct a team of 3-4 quality
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, participant recruitment and retention, data collection and management, coordination across interdisciplinary teams, and engagement with community and institutional partners. The role supports the efficient
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for the Graduate Student Center first floor information desk and Family Center visitor desk. As the first point of contact for many visitors, the Administrative Coordinator sets the tone for a positive experience by
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execution across leadership priorities. The Executive Assistant exercises sound judgment in managing competing requests, handling confidential information, and supporting executive workflows. While the Vice
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information about the Division of Business Services, visit: https://www.business-services.upenn.edu About Penn Ice Rink The University of Pennsylvania Class of 1923 Ice Skating Rink, located adjacent to the
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of Pennsylvania is a pioneering interdisciplinary research lab dedicated to applying computational methods and large-scale data to some of the most pressing challenges facing society. Founded and led by Duncan
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, collecting and reporting research data, accessing and reporting AE/SAEs per protocol, managing subject treatment per protocol, oversight and coordination of research testing, including labs, office visits and
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deficiencies and design and implement changes to mitigate risks. Manage communication and information flow with departments and stakeholders; provide exceptional customer service by responding promptly
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. Ensure study/trial data integrity and regulatory compliance with GCP guidelines, Federal/FDA regulations, and institutional/sponsor requirements. Supervise CRCs and CRNs as assigned. Supporting project
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, deviation/exception requests. Manage collection of data from source documents pertaining to study visits and transcribe to case report form, including concomitant medications and adverse events