Senior Clinical Data Risk Analyst

Meet Life Sciences; Torrejón de Ardoz; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading global CRO is seeking a Senior Clinical Data Risk Analyst to assess and mitigate clinical trial data risks. This role involves cross-functional collaboration, developing monitoring plans, and ensuring compliance, all while contributing to innovative therapies in a dynamic environment. Candidates should have significant experience in clinical risk management and data analysis, with opportunities for remote or hybrid work.

Formación

• 5+ years of experience in RBQM/clinical risk management.
• 7+ years in the pharmaceutical or clinical research industry.
• Proven experience leading global projects.

Responsabilidades

• Lead clinical data evaluations to identify risks and trends.
• Drive study-level risk assessments and central monitoring discussions.
• Collaborate with teams to implement risk mitigation strategies.

Conocimientos

Risk-Based Quality Management (RBQM)

Data Analysis

Stakeholder Management

Communication

Educación

Advanced degree in Biostatistics, Data Science, Life Sciences, or related field

Herramientas

CluePoints

Elluminate

Descripción del empleo

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.