Remote Clinical Data Risk Analyst for Trials

ICON Strategic Solutions; Argentina; Presencial; ARS 1.200.000 - 1.800.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Life insurance

Flexible country-specific benefits

Descripción de la vacante

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Clinical Data Risk Analyst at ICON, you will identify and mitigate risks associated with clinical trial data, ensuring data integrity and regulatory compliance across trial programs.

Formación

• Degree in statistics, life sciences, or a related field.
• Experience in clinical data analysis or risk management in a clinical research environment.
• Strong analytical skills and proficiency in statistical software and risk assessment methodologies.

Responsabilidades

• Conduct risk assessments on clinical trial data to identify issues and mitigation options.
• Collaborate with cross-functional teams to develop and implement risk management plans and protocols.
• Monitor data quality and integrity throughout the trial, reporting findings to stakeholders.
• Use statistical analysis and visualization tools to communicate risk insights effectively.
• Prepare risk management documentation for regulatory submissions and audits.

Conocimientos

Statistical analysis

Risk assessment

Data quality management

Communication

Team collaboration

Educación

Degree in statistics or life sciences

Herramientas

Statistical software

Descripción del empleo

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Clinical Data Risk Analyst at ICON, you will identify and mitigate risks associated with clinical trial data, ensuring data integrity and regulatory compliance across trial programs.