Central Monitor II (RBQM / KRI review Exp)

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Central Monitor II (RBQM / KRI Review Exp) based in India. This role offers the opportunity to support risk-based quality management across clinical research studies in a global life sciences environment. You will contribute to centralized monitoring activities by reviewing study data, identifying trends, and assessing risks at study, country, and site levels. Working alongside Central Monitoring Leads and multidisciplinary study teams, you will help ensure that emerging data quality and performance issues are identified and addressed promptly. You will use analytical tools to conduct data risk reviews, manage risks and issues, and maintain clear oversight of study parameters. The position combines clinical research expertise, data analysis, risk assessment, and stakeholder communication. It is well suited to an experienced central monitoring professional who is comfortable working with RBQM processes and KRI reviews.

Support the Central Monitoring Lead with study-specific setup, configuration, and ongoing maintenance of data analytics tools used for centralized monitoring. Act as a subject matter resource for RBM data analytical tools and use them to conduct data risk reviews and support risk and issue management. Perform centralized monitoring of clinical study data in accordance with the study monitoring plan. Maintain oversight of risk parameters and relevant indicators at study, country, and site levels. Review Key Risk Indicators (KRIs) and identify trends that may indicate systematic data errors, data quality concerns, or study, country, or site performance issues. Analyse monitoring findings and assess their potential implications for study quality, data integrity, and operational performance. Communicate trends, findings, risks, and recommendations clearly to relevant study team members. Document recommended actions and follow-up activities within the appropriate data analytical and monitoring tools. Provide regular status updates and reporting to study teams regarding centralized monitoring activities, identified risks, and issue resolution. Ensure that in-stream data reviews, risk assessments, findings, and issue management activities are properly documented and archived. Support the training of central and local study teams on RBQM principles, centralized monitoring processes, and relevant analytical tools. Share responsibility for maintaining data quality and risk oversight across study, country, and site levels. Collaborate with cross-functional clinical teams to support timely identification, escalation, and resolution of emerging risks. Requirements Minimum 2 years of relevant experience in Central Monitoring or a closely related clinical research role. Practical experience working with Risk-Based Quality Management (RBQM) processes and centralized monitoring methodologies. Experience reviewing Key Risk Indicators (KRIs) is strongly preferred. Experience with CluePoints or similar clinical data analytics and risk-monitoring platforms is advantageous. Understanding of clinical trial data, monitoring processes, data quality principles, and study risk management. Ability to analyse complex study data and identify trends, anomalies, systematic errors, and potential performance risks. Strong understanding of risk and issue management within clinical research environments. Ability to translate analytical findings into clear recommendations and actionable follow-up activities. Strong written and verbal communication skills, with the ability to communicate effectively with multidisciplinary and geographically distributed study teams. Excellent attention to detail and strong documentation skills, particularly when maintaining audit-ready monitoring records. Ability to work independently while collaborating effectively with Central Monitoring Leads and broader clinical study teams. Strong organisational and time-management skills, with the ability to manage multiple monitoring activities and priorities. Willingness and availability to work according to EMEA-aligned working hours. Benefits Fully remote working opportunity from India. Full-time position within a global clinical research and life sciences environment. Opportunity to work on international clinical studies and contribute to data quality and patient-focused research outcomes. Exposure to advanced RBQM, centralized monitoring, KRI review, and clinical data analytics practices. Opportunities to work with specialist data analytics and risk-monitoring technologies. Access to professional development and career progression opportunities. Technical and therapeutic-area training to strengthen clinical research expertise. Supportive line management and opportunities for peer recognition. Collaboration with multidisciplinary teams of clinical research and life sciences professionals across global markets. Opportunity to develop expertise in risk-based monitoring, data quality, risk management, and clinical study oversight. Inclusive working environment focused on collaboration, continuous learning, and professional growth.

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