Clinical Research Monitor(CRA)

Clinical Research Monitor Job ID: 26374 Location: Remote (Preferred Central U.S.) Duration: 24 Months Pay: $40–45/hr on W2 Key Requirements: Bachelor's degree required 3+ years Clinical Research/CRA monitoring experience Must travel up to 80% (primarily air travel) Knowledge of: FDA 21 CFR 812 ISO 14155 GCP/SOP compliance Experience with: CTMS RAVE Veeva MS Office Suite Responsibilities: Monitor clinical trial sites and ensure protocol/GCP/regulatory compliance Work with investigators, hospitals, CROs, and research sites Review adverse events, study data, budgets, timelines, and reports Train site staff and investigators Support study startup, monitoring, recruitment, and retention activities Maintain study documentation and status reporting Preferred: Medical device clinical trial experience Strong communication and organizational skills Ability to work independently in a remote environment Artech