Clinical Research Coordinator II
About The Position
The Center for Healthcare Delivery Science (CHDS) at Nemours Children’s Health in Delaware is seeking a full-time Clinical Research Coordinator II (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 sickle cell disease research under the direction of Aimee Hildenbrand, PhD. This position is based at Nemours Children’s Hospital – Delaware in Wilmington. The CRC will be responsible for leading the coordination and implementation of an NIH-funded trial testing a shared decision-making intervention for adolescents and young adults with sickle cell disease and their healthcare providers.
Requirements
- Minimum of a bachelor’s degree in psychology, pre-med, public health, or related
- Must be able to effectively use Microsoft computer software, SPSS, and REDCap
- Must be able to coordinate and establish priorities among diverse tasks
Nice To Haves
- Previous experience with providing research coordination for clinical trials
- Overseeing other research staff
- 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, Co-Investigators, and Community Advisory Board for the study
- Conducting trial site monitoring visits
- Ensuring that the study runs smoothly by problem-solving any issues with screening, recruitment, or data collection as they arise
- Engaging in qualitative and quantitative data collection and analysis
- Presenting at regional and national scientific meetings
- Helping prepare manuscripts for publication
- Receiving ongoing, individualized mentorship around career advancement
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
