
Clinical Trials Data Assurance Specialist
5 days ago
The Central Monitor II plays a vital role in guaranteeing the reliability and accuracy of clinical trial data through centralized monitoring activities, statistical analysis, and proactive risk management.
Main Responsibilities:- Develop and Implement Risk-Based Quality Management Plans
- Conduct thorough study risk assessments, identify potential issues, and develop mitigation strategies to ensure seamless clinical trials.
- Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, promoting proactive oversight.
- Ensure the highest standards of data quality and integrity by implementing timely interventions and collaborating with cross-functional teams.
- Bachelor's Degree in a relevant field (life sciences, statistics, data management)
- Minimum 2 years experience in clinical monitoring, clinical trial management or equivalent
- Familiarity with ICH GCP guidelines and the clinical development process
Qualifications Summary: The ideal candidate will possess strong analytical skills, excellent communication abilities, and the ability to work effectively in a team environment.
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