Senior Statistical Analyst
Icon Clinical PLC
Industria de Investigación Farmacéutica
Barcelona, Cataluña - Spanien
Project Manager Sénior / Especialista sénior
Experteer Overview
In this role, you will design and analyze clinical trial data to inform decisions and regulatory submissions. You will collaborate with cross-functional teams to develop statistical methods and analysis plans, build and validate models, and provide expert guidance on study design and data interpretation. You will contribute to statistical analysis protocols and programming specifications, helping advance innovative therapies. This position combines hands-on analysis with strategic input to shape trial outcomes and support ICON’s mission in clinical development. A strong balance of technical excellence and cross-team collaboration will enable you to impact decisions across programs and geos.
Compensaciones / Beneficios
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
Responsabilidades
- Collaborate with cross-functional teams to design statistical methodologies and analysis plans for clinical trials
- Conduct statistical analyses and interpret results to support decision-making and regulatory submissions
- Develop and validate statistical models to analyze clinical trial data and evaluate treatment outcomes
- Provide statistical expertise and guidance to support study design, protocol development, and data interpretation
- Contribute to the development of statistical analysis protocols and programming specifications
Requisitos principales
- Master's or Ph.D. degree in Statistics, Biostatistics, or related field
- Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry
- Proficiency in statistical software such as SAS, R, or Python
- Strong understanding of clinical trial design, statistical methodologies, and regulatory requirements
- Excellent analytical, problem-solving, and communication skills
Descripción del puesto
In this role, you will design and analyze clinical trial data to inform decisions and regulatory submissions. You will collaborate with cros…
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