Job Description Summary

The Clinical Research Coordinator A will assist in the management of multiple clinical trials and responsibilities in specific research areas. Coordinate the screening of patients and subject enrollment for one or more federally-funded studies in a fast-paced inpatient hospital setting; screen/enroll eligible subjects 5 days/week, in-person; obtain informed consent from study subjects or their proxies (in-person or by phone); human specimen collection (anatomical and environmental swabs) with hospital subjects; specimen collection from healthcare workers and other hospital staff; coordinate specimen tracking and drop off with research laboratory staff; coordinate study operations with staff; ensure protocol compliance; data abstraction from medical records; data entry, maintain patient and data tracking system; participate in the development of study materials and procedures; participate in weekly research team meetings. This position involves working in the hospital and spending the majority of the workday on the hospital units. This position also involves collection and coordination of biological samples with transport to the microbiology laboratory as well as coordination of study activities with data management. Collection and coordination of biological samples require extreme flexibility within the daily work schedule. This position reports directly to the study's project manager. This position may require flexibility to work occasional nights/weekends.

Job Responsibilities

• Determination of subject eligibility upon detailed review of medical chart via EPIC; assembling study enrollment packets.
• Approach all eligible subjects every weekday and obtain informed consent.
• Collection of multiple sets of human or environmental specimens on two hospital units (nose, throat, groin swabs and hand cultures)
• Medical Chart Abstraction (using multiple hospital databases) - Data to be collected will include: patient demographics, clinical and laboratory data, vital signs, medications. Data Entry into study database / database management
• Coordination of biological specimen collection and transport that involves labeling & organizing specimens; Attend web-based or in-person meeting to discuss data
• Other duties and responsibilities as assigned

The appointment will run through December 31, 2026. Continuation beyond this date may be possible if additional funding becomes available.