670 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UNIV" "Univ" "Univ" positions at University of Pennsylvania
Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
on the candidate’s qualifications, experience, skills, and education as they directly relate to the requirements of the position, and in alignment with salary ranges based on external market data for the job’s level
-
Research Coordinator A (Affective Disorders Program) Job Profile Title Clinical Research Coordinator A Job Description Summary This position will assist in the management and data collection of multiple
-
, coordination of clinical trials, including recruiting new patients, maintaining high retention levels, interviewing participants, gathering medical data, coordinating visits with, interdepartmental units
-
. Provides complex administrative support, including arranging logistics for events, drafting correspondence and reports, researching topics, performing routine data analysis, and maintaining budgets. Job
-
operates, reconciles, and reports on volumes and statuses of Mailroom through-put. The Lead Tech oversees BSA proper use of the automated tracking system, cognizant of maintaining data integrity and
-
study reports that cover project development, research design, data collection, and quantitative analyses; assisting the research team in preparing manuscripts, publications, and grant applications
-
reports that cover project development, research design, data collection, and quantitative analyses; assisting the research team in preparing manuscripts, publications, and grant applications; training and
-
. Leveraging data analytics to inform strategic decision-making and drive operational excellence. Provide expert guidance on HR policy, compliance, and workplace challenges while contributing to a positive and
-
services Support radiation oncology clinic operations, including appointment coordination and consultation requests Participate in clinical research activities, including data collection and maintenance
-
compliance; assisting with the preparation and submission of IRB documents for clinical trials; helping to prepare for study monitoring visits; completing data entry and query resolution; and assisting with