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1 week ago
The Central Monitor II plays a pivotal role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.
- Main Responsibilities:
- Lead the development of Risk-Based Quality Management plans to ensure high standards of data quality and integrity.
- Conduct study risk assessments, identifying potential issues and developing mitigation strategies to minimize risks.
- Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks.
- Collaborate with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management.
- Bachelor's Degree: In a relevant field or equivalent combination of education, training, and experience.
- Work Experience: Minimum 2 years in clinical monitoring, clinical trial management or equivalent.
- Skills and Knowledge: Working knowledge of ICH GCP guidelines and the clinical development process. Statistical analysis and data monitoring skills are essential.
This role requires strong analytical skills, attention to detail, and effective communication skills. If you are passionate about ensuring the accuracy and integrity of clinical trial data, we encourage you to apply for this exciting opportunity.
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