Chief Data Integrity Specialist

11 hours ago


Dindigul, Tamil Nadu, India beBeeClinical Full time ₹ 1,00,00,000 - ₹ 1,25,00,000
Job Role Overview

The Central Monitor II is a key professional responsible for ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.

Main Responsibilities
  • Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies.
  • Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
  • Support monthly RBQM meetings by reviewing study data, documenting findings, action plans, and coordinating data cleaning activities.
  • Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
  • Collaborate with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management and data cleaning for studies.
  • Prepare detailed reports and presentations on monitoring activities, findings, and recommendations for sponsors and study teams.
Key Qualifications
  • Bachelor's Degree in a relevant field (life sciences, statistics, data management, clinical operations) or relevant/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.
Essential Skills
  • Statistical analysis and data monitoring.
  • Risk assessment and mitigation.
  • Report writing and presentation.
  • Collaboration and teamwork.


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