Social/Clinical Research Assistant
About The Position
The Division of Allergy and Immunology serves the children of North Carolina in the diagnosis and treatment of known or suspected immune deficiencies and allergic diseases, including food and environmental allergies. Within the Division, established and anticipated research studies conducted by the Food Allergy Initiative (FAI) supports a nationally recognized program. The program is dedicated to the study of new medicines and treatments, laboratory studies involving allergies and desensitization (mice and human subjects), and the education of community physicians, allied health professionals, and the public. This position will serve as a Research Assistant to Dr. Corinne Keet within the UNC FAI. The Research Assistant is responsible for coordinating participant-facing research activities, including screening and recruiting participants, obtaining informed consent, scheduling and conducting study visits, collecting study data, performing non-licensed clinical procedures, and serving as a liaison throughout study participation. This position also supports study data management and analysis through database creation, data entry, quality assurance, report generation, statistical analysis, and documentation of protocol deviations, discrepancies, and adverse events.
Requirements
- Experience in coordinating participant-facing research activities
- Experience in screening and recruiting participants
- Experience in obtaining informed consent
- Experience in scheduling and conducting study visits
- Experience in collecting study data
- Experience in performing non-licensed clinical procedures
- Experience in serving as a liaison throughout study participation
- Experience in supporting study data management and analysis
- Experience in database creation
- Experience in data entry
- Experience in quality assurance
- Experience in report generation
- Experience in statistical analysis
- Experience in documentation of protocol deviations, discrepancies, and adverse events
Responsibilities
- Coordinating participant-facing research activities
- Screening and recruiting participants
- Obtaining informed consent
- Scheduling and conducting study visits
- Collecting study data
- Performing non-licensed clinical procedures
- Serving as a liaison throughout study participation
- Supporting study data management and analysis
- Database creation
- Data entry
- Quality assurance
- Report generation
- Statistical analysis
- Documentation of protocol deviations, discrepancies, and adverse events
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
