Clinical Research Professional
1 dia atrás
As a seasoned clinical research professional, you will be part of a dynamic team driving the world's largest and most comprehensive clinical research organization forward.
Key Responsibilities:- Efficiently manage multiple priorities and responsibilities with increasing scope and complexity.
- Utilize strong planning and organizational skills to ensure seamless work execution.
- Proactively deliver quality work under pressure while maintaining a proactive approach to issue analysis and conflict resolution.
- Effectively travel to assigned locations as required.
- Successfully execute local study setups and close-outs with high-quality results.
- Perform operational site evaluation visits, study initiation visits, on-site monitoring visits at required frequency, and site close-out.
- Assess feasibility of study protocol with reference to study complexity.
- Verify staff availability, suitable clinical facilities, and potential for per-protocol patient population.
- Ensure compliance with ICH-GCP requirements and verify data entered into CRFs is consistent with patient medical notes and entered in real-time.
- Maintain good relationships with sites and ensure critical study timelines are achieved.
- Verify Investigator and site staff receive safety reports and new safety information in a timely manner.
- Accurately collect and provide safety data within required time frames.
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