Data Integrity Specialist

5 days ago


Anand, Gujarat, India beBeeClinicalMonitor Full time ₹ 90,72,000 - ₹ 1,21,20,000

The Central Monitor II role is a critical position in ensuring the quality and integrity of clinical trial data.

Key Responsibilities:
  • Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies, in consultation with functional team leads and PM.
  • 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 to support study deliverables.
  • Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
  • Collaborate closely 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.
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.


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