We are partnering with a leading global CRO to support the search for a Senior Clinical Data Risk Analyst. This is a unique opportunity to join a world-renowned organisation at the forefront of clinical research, contributing directly to the development of innovative therapies and ensuring data quality through expert risk-based monitoring.As a Senior Clinical Data Risk Analyst, you’ll take a central role in assessing and mitigating clinical trial data risks across multiple global studies. You’ll work cross-functionally with clinical teams to develop central monitoring plans, ensure regulatory compliance, and guide data-driven decision-making.Key ResponsibilitiesLead clinical data evaluations to identify risks and trends affecting study outcomesDrive study-level risk assessments and central monitoring discussions with global study teamsReview and interpret KRIs, QTLs, and statistical monitoring outputs across regionsDevelop study-specific central monitoring and data surveillance strategiesServe as the primary contact and subject matter expert for statistical monitoring toolsCollaborate with cross-functional teams to implement risk mitigation strategiesOversee the analysis of data discrepancies and provide insights to inform key decisionsPromote compliance and data governance best practices across clinical operationsMaintain central monitoring documentation and contribute to audit readinessIdeal Candidate Profile5+ years of professional experience specifically within RBQM / clinical risk management7+ years of total experience in the pharmaceutical or clinical research industryProven experience leading global projects within RBQM or central monitoringStrong, hands-on experience with either CluePoints (RBM) or Elluminate (EDC) – both not requiredData-focused profile – candidates must have direct experience with analytics and system use (not oversight only)Advanced degree in Biostatistics, Data Science, Life Sciences, or related fieldStrong knowledge of KRIs, QTLs, and central monitoring methodologiesExcellent communication and stakeholder management skillsThis role offers the opportunity to work in a global, dynamic environment with the flexibility of remote or hybrid working within Poland. You’ll be instrumental in shaping risk strategies that directly support the delivery of safe, high-quality clinical trials.Interested in learning more? Apply today or reach out for a confidential discussion.