Clinical Research Coordinator I

Participant Coordination, Visit Execution, and Basic Clinical Support: Following detailed instruction, will recruit, screen, consent, and schedule study participants. With instruction, prepare visit materials and assist with visit flow for physical assessments (e.g., 6MWT, active stand, anthropometrics, EKG). With guidance, provide participant education within defined limits. Coordinate referral-based procedures. Under direction, conduct routine study-required clinical support tasks (specimen handling, vitals, basic AE documentation with escalation). Following established protocol, maintain participant engagement through reminders, follow-up communication, and assistance with retention activities. Execute administrative scheduling tasks for both studies, including tracking reschedules and missed visits. Survey Distribution, Data Collection, and Data Entry: As directed, send scheduled surveys and follow established communication policies. Enter data into electronic databases with attention to completeness, accuracy, and adherence to data management procedures, under supervision. Assist with basic data quality checks and tracking logs. Support proper specimen labeling, processing, and chain-of-custody documentation according to protocol requirements. Technical Duties: Under direct supervision, assists in performing flow-mediated dilation on research participants. Assist in performing pulse wave velocity on research participants, under supervision. Under direction of PI, assist with collecting and processing blood samples per established protocol. Knowledge, Skills Abilities: Knowledge of ethics and regulations for human subjects research. Strong interpersonal skills and excellent communication. Phlebotomy skills. Knowledge of medical terminology and conditions. Detail oriented with strong organizational skills.