Senior Clinical Data Risk Analyst

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 Responsibilities

• Lead clinical data evaluations to identify risks and trends affecting study outcomes
• Drive study-level risk assessments and central monitoring discussions with global study teams
• Review and interpret KRIs, QTLs, and statistical monitoring outputs across regions
• Develop study-specific central monitoring and data surveillance strategies
• Serve as the primary contact and subject matter expert for statistical monitoring tools
• Collaborate with cross-functional teams to implement risk mitigation strategies
• Oversee the analysis of data discrepancies and provide insights to inform key decisions
• Promote compliance and data governance best practices across clinical operations
• Maintain central monitoring documentation and contribute to audit readiness

Ideal Candidate Profile

• 5+ years of professional experience specifically within RBQM / clinical risk management
• 7+ years of total experience in the pharmaceutical or clinical research industry
• Proven experience leading global projects within RBQM or central monitoring
• Strong, hands-on experience with either CluePoints (RBM) or Elluminate (EDC) – both not required
• Data-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 field
• Strong knowledge of KRIs, QTLs, and central monitoring methodologies
• Excellent communication and stakeholder management skills

This 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.