
Clinical Data Specialist
10 hours ago
The Central Monitor II plays a pivotal role in ensuring the accuracy and reliability of clinical trial data through centralized monitoring activities, statistical data analysis, and proactive risk mitigation.
Key Responsibilities- Conduct thorough assessments to identify potential risks and develop effective strategies for mitigation.
- Perform comprehensive statistical reviews and data analysis to detect anomalies and trends.
- Support regular review meetings by analyzing study data, documenting findings, and coordinating cleaning activities.
- Maintain the highest standards of data quality and integrity through proactive monitoring and timely interventions.
- Bachelor's Degree in a relevant field (life sciences, statistics, data management) or equivalent combination of education, training, and experience.
- Minimum 2 years experience in clinical monitoring, clinical trial management, or equivalent.
- Working knowledge of ICH GCP guidelines and the clinical development process.
- CRO experience as a Central Monitor.
Skills: Statistical analysis, Risk assessment, Report writing, Collaboration and teamwork.
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Clinical Data Specialist
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Clinical Data Expert
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Clinical Data Specialist
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Clinical Data Specialist
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Clinical Data Programming Specialist
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Clinical Study Document Specialist
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Clinical Research Specialist
6 days ago
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