683 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Here We Are" positions at University of Pennsylvania in United States
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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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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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through facility upgrades and expansions Learn more: https://business-services.upenn.edu About Penn Children's Center: Penn Children’s Center provides high-quality early childhood education for children
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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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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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Coordinator will oversee the collection of MRI data from recruitment through quality assessment and data analysis. Job Description The Perelman School of Medicine at the University of Pennsylvania is the
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on specific experimental techniques as necessary. The Research Investigator will also contribute to data analysis, preparation of manuscripts and grant applications, and presenting research findings through
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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