Clinical Central Monitor

2 months ago


City of London Greater London, United Kingdom Proclinical Staffing Full time

Proclinical is seeking a Central Monitor Lead with a strong data analytics aptitude. This role is integral to driving customer success and broad adoption of our advanced statistical algorithms for clinical trial data quality. Guide data analysts in reviewing Central Monitoring Platform outputs and performing initial investigations of identified risks.
Summarize findings and communicate results to clients, ensuring they understand the impact on their data.
Coach clients' Risk Coordinators in the Signal Management process, defining appropriate follow-up actions and ensuring robust documentation.
Support study teams in adopting an approach to clinical trial monitoring that focuses resources on risks with the most potential to impact patient safety and data quality.
Participate in the continuous improvement and development of our product solutions and operational processes.

Previous experience with and understanding of clinical trials and clinical data across multiple therapeutic areas.
Previous experience within clinical operations and understanding of key processes including monitoring, data management, (medical) data review and related processes.
Aptitude for data analytics and critical thinking skills to determine the signs of risk.
Effective English verbal and written communication skills in relating to people both inside and outside the organization in a team environment.
Works independently, ability to multi-task and provide expertise on multiple projects concurrently.
Bachelor's degree or above in a scientific or business-related discipline required.
Proven working experience in RBQM/Central Monitoring.



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