Research Ethics (Studies) Coordinator
Core
Administrative and scientific coordination of research ethics board submissions, reviews, and approvals for biomedical research protocols.
Role type
Senior Research Ethics Coordinator (IC)
Builds
Ethical compliance and regulatory documentation for clinical trials and biomedical research studies.
Domain
Healthcare research administration and bioethics
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Research protocol review, regulatory framework knowledge (Tri-Council, ICH-GCP, FDA, PHIPA), electronic document management, research methodology, stakeholder liaison
Preferred skills
Clinical research certification (SOCRA/ACRP), bioethics knowledge, volunteer REB committee experience, electronic REB system experience (CAPCR/Romeo/Infonetica)
Technologies
Microsoft Office, Teams, Adobe Reader, electronic REB application systems
Responsibilities
Coordinate and review REB submissions and study documents; Act as ethics liaison with REB members and investigators; Document REB discussions and decisions; Maintain and archive electronic research files; Attend REB meetings.
Seniority
Mid-Senior, hands-on IC