Experience working with datasets, including data processing and organization.
Comfort with basic handling of rodent models and tissue samples for experimental procedures.
Previous experience with physiological data collection and common wet lab techniques (e.g., Western blotting, RT-PCR, ELISA, histology).
Familiarity with clinical research procedures, including participant enrollment and informed consent.
Strong organizational skills, intellectual curiosity, and keen attention to detail are essential.
Competencies
Demonstrate strong attention to detail, accurate data entry skills, and intermediate computer proficiency (including experience with Microsoft Office and Adobe software). Effective time management and the ability to multitask in a dynamic environment.
Target Compensation Maximum:
$70,623.00 Target Compensation Minimum:
$47,048.00 Compensation will be commensurate to candidate experience.
Equal Employment Opportunity
Consistent with applicable law, demographic information is collected for aggregate reporting requirements. Demographic information provided through this application is not available to hiring managers/committees and is not considered in hiring or employment decisions.
Assistance and Accom
Benefits
Health insurance
Additional Information
Department:
Location:
Health Sciences Center Time Type:
Full time Worker Type:
Regular Job Req ID:
R108716 Minimum Requirements:
Bachelor's degree in a related field and two (2) years relevant research experience or an equivalent combination of education and experience. Grade 5 (Salaried) Position Description:
The Department of Otolaryngology-Head & Neck Surgery and Communicative Disorders at the University of Louisville School of Medicine is seeking a full-time Research Coordinator V. This position will support research initiatives led by multiple Principal Investigators in the areas of speech-language pathology and head and neck cancer. The research focuses on biomolecular and physiological measurements in humans, live rodents, and tissue samples. Key responsibilities include coordinating laboratory activities, managing data collection and analysis, and ensuring the efficient operation of ongoing experiments. Opportunities to assist with grant applications may also be possible and may include pre-award and post-award responsibilities such as completion of forms, formatting and verification of accuracy of documentation, verification of application completeness, assistance with budget development and post-award budgetary management, and other post-award project management tasks. It is generally anticipated that the individual will spend about 20 hours per week engaged in the wet lab and the remaining 20 hours/week coordinating study activities, including participant recruitment and data curation.
Essential Duties and Responsibilities
Identify and recruit participants for clinical/observational studies, obtain informed consent, collect study data, and coordinate or track study activities.
Collect and process human and rodent tissue samples for analysis.
Acquire and analyze physiological data from humans and rodents (e.g., swallow studies).
Handle laboratory rodents and collect physiological data.
Organize, analyze, and summarize large experimental datasets using MS Excel, REDCap, and/or other data management and processing software.
Perform biochemical and molecular assays (e.g., histology, Western blot, RT-PCR, ELISA).
Prepare materials and equipment required for laboratory tests and experiments.
Manage tasks and coordinate research efforts across multiple Principal Investigators
Assist with funding acquisition and post-award management tasks
Uofl · Health Sciences Center