Bilingual (Spanish/English) Clinical Research Coordinator
About The Position
The Center for Healthcare Delivery Science (CHDS) at Nemours Children’s Health in Delaware is seeking a full-time Bilingual (Spanish/English) Clinical Research Coordinator (CRC). The CHDS is a research center across the Nemours enterprise. The CHDS includes over 20 investigators that study ways to improve health care, health equity, and health and wellness beyond medicine for youth and their families. Research projects span a variety of medical conditions (e.g., cancer, sickle cell disease, diabetes, pain, asthma, food allergy, disordered eating) and other health-related challenges (transition from pediatric to adult healthcare, behavioral interventions to improve coping with disease and treatment demands). This specific CRC position will support Type I diabetes research under the direction of Paul Enlow, PhD. This position is based on site at Nemours Children’s Hospital – Delaware in Wilmington. The CRC will be responsible for the coordination and implementation of two NIH-funded clinical trials of a multicomponent intervention to improve engagement with diabetes technologies among adolescents with type 1 diabetes. One study focuses specifically on adolescents from families who are primarily Spanish-speaking.
Requirements
- Minimum of a bachelor’s degree in psychology, pre-med, public health, or related field
- Fluent bilingual (English/Spanish) communication skills are required
- Must be able to effectively use Microsoft computer software, SPSS, and REDCap
- Must be able to coordinate and establish priorities among diverse tasks
- Previous experience with providing research coordination for clinical research is required
Nice To Haves
- Reliable transportation
- A two-year commitment
Responsibilities
- Coordinating IRB submissions
- Maintaining an up-to-date study regulatory binder
- Reviewing documentation for study recruitment and completion
- Monitoring participant status in relevant databases
- Organizing participant payments
- Maintaining regular contact with research coordinators across the trial sites
- Attending meetings with the Principal Investigator and Co-Investigators for the study
- Helping to ensure that the study runs smoothly by problem-solving any issues with screening, recruitment, or data collection as they arise
- Engage in qualitative and quantitative data collection and analysis
- Present at regional and national scientific meetings
- Help prepare manuscripts for publication
- Receive ongoing, individualized mentorship around career advancement
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
