Central Monitoring Lead

23 hours ago


Bengaluru, Karnataka, India beBeeRisk Full time ₹ 75,00,000 - ₹ 1,00,00,000

Senior Central Monitor Role

The Senior Central Monitor is a crucial position in ensuring the integrity and quality of clinical trial data through centralized monitoring, statistical review, and risk management.

  • Key Responsibilities:
  • Lead the development of comprehensive Risk-Based Quality Management (RBQM) plans tailored to each study's needs, collaborating with cross-functional teams.
  • 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.
  • Facilitate monthly RBQM meetings by supporting review of study data, documenting findings, action plans, and coordination of data cleaning activities.
  • Ensure 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.
  • Prepare detailed reports and presentations on monitoring activities, findings, and recommendations.
  • Oversee operational study metrics, including data entry trends, SDV backlog, site health trending, and communicate issues proactively to study team members.

Requirements and Qualifications:

  • Proven experience in central monitoring and risk-based quality management.
  • Strong analytical and problem-solving skills.
  • Excellent communication and collaboration skills.
  • Ability to lead cross-functional teams and facilitate effective meetings.

Benefits:

  • Opportunity to work on high-profile clinical trials.
  • Professional growth and development opportunities.
  • Competitive compensation and benefits package.

About this Role:

This role offers a unique opportunity to make a significant impact on the quality and integrity of clinical trial data. If you are a motivated and detail-oriented individual with experience in central monitoring and risk-based quality management, we encourage you to apply.



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