Clinical Research Coordinator
Core
Coordinate clinical trial conduct, manage participant interactions, and ensure regulatory compliance for study integrity.
Role type
Clinical Research Coordinator
Builds
Clinical trials for medical research
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Protocol adherence, data collection, informed consent administration, adverse event documentation, clinical procedures (EKGs, vital signs), regulatory file maintenance, EDC data entry, participant recruitment support
Preferred skills
Analytical reasoning, attention to detail, organizational skills, stakeholder communication, multi-priority management
Technologies
Electronic Data Capture (EDC) systems, electronic source (eSource) documents
Responsibilities
Monitor participant health and compliance, collect medical history and concomitant medication data, document adverse events, perform clinical assessments, maintain investigational product records, coordinate laboratory testing, manage study startup documentation, enter and resolve data in EDC systems
Seniority
Mid-level, hands-on IC
