TheQACE Analystrole is a critical . Additionally, the candidate will be responsible for creating trackers to monitor findings.DUTIES & RESPONSIBILITIESAnalyze clinical data obtained from various sites and identify trends, findings, and anomalies that could impact data quality and regulatory compliance.Create cross-functional tools to analyze and visualize data trends and anomalies and enhance analysis and reportingCollaborate with various teams, such as, site leadership, clinical investigators and other research staff to ensure data integrity and qualityPresent findings to stakeholders and communicate recommendations for corrective action plans.Collaborate with site staff to implement corrective action plans and monitor the effectiveness of these plans.Ensure adherence to ALCOA+, GDP, GCP Standards with all relevant clinical trial documentation.Conduct training for site staff on data collection, management, and analysis.Create cross-referencing trackers with ability to generate reports for Quality Assurance and ClinicalvExcellence (QACE).Communicate with new or established sites, functional teams to collect and analyze data.Identify trends and patterns which may have a potential impact on study outcomes and communicate tovstakeholders in a clear an conciser matterAssist in the training of new QACE team members.Submit required administrative paperwork per company timelines.Any other matters, as assigned by management.KNOWLEDGE & .....Knowledge of basic use of scientific methods, procedures, and techniques.Exceptional problem solving skills, and root cause analysis of issues.Flexibility to travel up to 10% of the time.Ability to work independently and as part of a team.Strong communication, organizational, and interpersonal skills.