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.