Clinical Research Coordinator II, Surgery
Core
Manages moderately complex clinical trials in surgery, recruiting subjects, collecting data/samples, and ensuring regulatory compliance.
Role type
Clinical Research Coordinator II (IC)
Builds
Clinical research studies for pharmaceutical sponsors and internal research
Domain
Biomedical research / Clinical trials / Surgery
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, data collection and abstraction, adverse event reporting, protocol adherence, regulatory compliance (GCP, IRB), sample processing and storage, site visit coordination
Preferred skills
Multi-site trial coordination, ACRP or SoCRA certification, Good Documentation Practices (GDP), medical terminology knowledge, clinical trial protocol interpretation
Technologies
Microsoft Word, Excel, Adobe Acrobat
Responsibilities
Recruit and screen study subjects; collect, process, and store clinical samples; manage data integrity and quality assurance; coordinate sponsor visits and site audits; ensure compliance with federal regulations and institutional policies; mentor junior coordinators on GCP and SOPs
Seniority
Mid-level IC (2-5 years experience)