369 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"I.E" positions at University of Pittsburgh
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implementation of patient care. Observes, documents, and communicates to the physician and/or other clinical staff symptoms, potential problems, and pertinent information regarding patient care. - Charts doctor
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to presentation, including planning, organizing, conducting experiments, assessing protocol feasibility, processing, and analyzing data, and conference presentations. •Prepares complex manuscripts, research
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, effective communication with clinicians and other health professionals, data and compliance tracking, patient retention, and accurate reporting. Physical Effort This position requires availability to contact
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and clean or soiled bedding and caging with reasonable accommodations if necessary • Accurately and legibly document written information in English in a timely manner, including electronic formats and
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and data, reconcile transactions to the general ledger and other shadow systems, ensure University accounting standards are met, and identify opportunities to streamline business processes throughout
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of Indemnification and Local Context Forms. This position requires the employee to obtain information related to the types of agreements being requested, as well as making an initial determination regarding
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to advance the CEE department, and (6) Names and contact information for at least three professional references. The application material should be uploaded at www.join.pitt.edu (Requisition number 25006524
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information about BHAS, please visit our website at BHAS.pitt.edu or follow us on LinkedIn . Job Summary Operates point of sale system, reconciles tills and daily sales, processes exchanges and returns, and
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, collaborative spaces, and donor‑facing environments. • Develop policies for data governance, research integrity, cybersecurity, and safety. • Manage crisis response plans, operational continuity, and risk
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for clinical trials • Collects, maintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies. Several trials will