684 data "https:" "https:" "https:" "https:" "UCL" positions at University of Pennsylvania
Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
. 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
-
analyze results, including analyses of archived data, while adhering to standard procedures and guidelines. This position will manage all animal projects in CAMIPM. Duties include but not limited to carry
-
lab visits to assess CO, e-cigarette and cigarette use across 6 weeks; and (5) follow up with participants who reschedule or fail to show for an appointment, enter the study data, and ensure adequate
-
execution across leadership priorities. The Executive Assistant exercises sound judgment in managing competing requests, handling confidential information, and supporting executive workflows. While the Vice
-
documentation of workflows and contribute to data quality control to ensure reproducibility. The candidate will also be required to read relevant scientific literature to for establishing new technologies and
-
documentation- including source documentation, case report forms, and research charts. Collect, review and report study data, Complete case report forms and resolve data queries Participate in the initiation
-
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
-
, 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
-
are priorities, as is a commitment to helping others, tolerance for ambiguity, and sense of humor. Proficiency in using student information systems, advising platforms, and other educational technology tools is
-
samples; collecting and filing study documents; and collecting and entering clinical data. Utilizing a variety of electronic systems, the CRC will document study activities with accuracy. The coordinator