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Description Essential Job Responsibilities: Recruitment and coordination of trial subjects covering informed consent, screening subjects through inclusion and exclusion criteria, and adhering to safety and compliance issues Coordination and management of the clinical trial, generating source
Enforce compliance to AS9100D/ISO9001 and other Quality standards Manage Non-conformance tracking/analysis and reduction through meetings and communication with project leadership and MRB Lead compliance reviews Perform FMEA and RCCA for non-conforming products/processes Create and Audit work
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