340 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"Dr" positions at University of Pittsburgh
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, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues
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Database Admin III - PBC Health Sciences Core Research Facilities - Pennsylvania-Pittsburgh - (25006775) Evaluates business requirements, creates data ingestion processes and modeling, and supports
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, including test scores, immigration documents, and transcripts. Evaluates admissions applications and credentials from around the world. Verifies accuracy of documentation and data and resolves incomplete
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information on admissions standards, academic and non-academic programs, and student activities following established procedures and precedents. Resolves complex problems as necessary (i.e. danger to the guests
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to, recruiting and enrolling patients into studies, imaging techniques, and analyzing and interpreting data. You will be responsible for providing regular updates to collaborators/senior scientists. You will be
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autoimmune diseases Reproductive Experiences in Autoimmunity (REINA) patient registry, which collects longitudinal data from women with autoimmunity as they progress from reproductive age to menopause Job
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. · Conduct molecular cloning, transfection, viral packaging, and titration assays (qPCR/ddPCR). · Collaborate across research teams to design experiments and interpret data. · Present data during lab and
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manages the clinical placement process by overseeing the clinical affiliation agreement and student placement. Manages the web-based platform for clinical education information coordination. Ensures site
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studies. This includes testing for identity, purity, composition, integrity, safety, activity, stability, viability, and potency assays. Collect background information for testing/experiments/production
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Science is seeking a Clinical Research Coordinator III. The individual in this role will conduct and is responsible for all study-related activities, including screening and consent enrollments, data