Clinical Research Coordinator overseeing multi-site orthopedic clinical studies, providing comprehensive information and ensuring compliance with regulatory standards. Collaboration with researchers for study design and team training is key.
Responsibilities
Oversees and coordinates complex or multi-site clinical research studies for two clinical researchers.
Serves as a resource to provide comprehensive information to clinical research staff promoting a smooth operation, preparation of regulatory compliance, and interaction with other departments.
Acts as the primary liaison to PI in developing plans for research projects and discussing the interpretation of results.
Designs, implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies.
Provides guidance to members of research team in the implementation and evaluation of clinical research; trains new staff.
Requirements
Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
Clinical Research (3 Years)
Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements). BLS certification must be obtained within one month of hire date.
Skills: Supervision, Clinical Research Management, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)
Benefits
Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development opportunities
Job title
Senior Clinical Research Coordinator – Orthopedic Surgery
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