174 data-"https:" "https:" "https:" "https:" "https:" "https:" "SciLifeLab" "IFM" "IFM" positions at University of Louisville
Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
direction and oversight of the EAT Lab digital treatment research team serving as a liaison between the clinical and data science teams to translate evidence-based psychological interventions into accessible
-
for the comprehensive management, coordination, and data oversight of undergraduate and graduate academic programs within the School of Nursing. This position provides high-level programmatic, administrative, and
-
. Preferred Qualifications Strong project management skills Strong computer skills Physical access administration experience Knowledge of physical access control systems and video surveillance systems Familiar
-
Microsoft Office Customer Service Strong Communication and Presentation skills Experience with CRM Ability to review data Compensation will be commensurate to candidate experience. Equal Employment
-
supporting entities / laboratories to ensure prompt sample preparation and analysis on a regular weekly basis. Specific tasks include sample preparation and direct laboratory and data analysis to detect
-
organization, assisting with data collection in the lab, online, and in the clinic, assisting with grant applications, entering and coding data, supervising undergraduate and graduate assistants, maintaining
-
strategic oversight of all academic records, registration, enrollment operations, and student data systems at the University of Louisville. As the institution's official custodian of student records and
-
policy reporting and other agreement-specific requirements. Coordinate data collection and narrative development across multiple academic and administrative units to produce comprehensive, high-quality
-
bridge programs for undergraduate students. Maintains Math Resources and summer program data to assist with annual reports on the effectiveness of programs and services. ESSENTIAL DUTIES AND
-
reporting requirements; assists physicians in ensuring adequate source documentation and data-collection that validate the integrity of the clinical trial; assist in enhancing recruitment of study