Clinical Research Coordinator 2, Department of Surgery
Core
Manages moderately complex clinical trials, recruits and screens subjects, collects and processes research data/samples, and ensures regulatory compliance for biomedical research studies.
Role type
Senior Clinical Research Coordinator
Builds
Clinical research studies and data sets for pharmaceutical and investigator-initiated trials
Domain
Biomedical research / Clinical trials
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial management, subject recruitment and screening, informed consent administration, data collection and abstraction, adverse event reporting, protocol adherence monitoring, specimen processing and storage, regulatory compliance (GCP, IRB), data quality assurance, SOP implementation
Preferred skills
Multi-site trial coordination, ACRP or SoCRA certification, management and regulatory compliance certification, medical terminology knowledge, clinical trial protocol interpretation, IRB submission process understanding
Technologies
Microsoft Word, Excel, Adobe Acrobat
Responsibilities
Manage multiple moderately complex clinical trials including national and multi-institutional studies; recruit, screen, and enroll study subjects; collect, process, ship, and store clinical specimens; ensure data accuracy and integrity through quality assurance and audit resolution; identify and report adverse events and protocol deviations; maintain accurate regulatory records including informed consent and IRB approvals; mentor junior staff on clinical research basics.
Seniority
Mid-level, hands-on IC