Clinical Research Monitor(CRA)
Artech Information Systems LLC
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
Vacancy posted 2 days ago
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