Quality Control Associate

The opportunity
The Quality Control Associate works in conjunction with site staff to ensure clean, accurate, and quality-reviewed data from beginning to end of study.How you’ll spend your day
Performs all activities and procedures in strict compliance with the study protocol, Good Clinical Practice standards (GCPs), Good Documentation Standards (GDPs), Standard Operating Procedures (SOPs), QA/QC procedures, OSHA guidelines, and other applicable regulations.
Supports the clinical operations team in reviewing essential clinical documents for accuracy.
Assists in the development and implementation of quality control procedures and processes.
Collaborates with study teams to identify and resolve quality issues.
Records, tracks, and ensures resolution of data queries.
Understands protocol-driven timed study events and acceptable collection windows.
Proactively communicates issues and resolutions to departmental supervisors and managers.
Performs general administrative tasks as required.
Other tasks as assigned by management.