Principal Statistician - Lead Quantitative Strategy (Hybrid)

GSK; Siena; In loco; EUR 48.000 - 81.000; Tempo pieno

Vantaggi offerti da questo lavoro

Permanent contract

Smart Working 50%

Flexible benefits

Healthcare plan

Pension fund

Employee assistance programme

Vaccination clinic

Tax assistance

Nursery support

On-site gym

On-site canteens

Descrizione del lavoro

GSK in Siena, Italy is seeking a Principal Statistician to provide statistical leadership across study designs. You will influence protocol inputs, adaptive design considerations, and decision-making activities within multidisciplinary teams.

Qualifications include a Master’s or PhD in statistics or epidemiology and significant experience with R and clinical trial statistics. Fluency in English is required; Italian language skills are preferred.

Competenze

• Master's Degree in Statistics or related field with at least 5 years in pharma, or PhD with ≥2 years in pharma.
• Experience in statistical software (R preferred) and sample size computation for standard designs.
• Ability to work in multidisciplinary teams and communicate complex statistical concepts in English.

Mansioni

• Provide statistical expertise to support diverse study designs.
• Lead activities to progress career and drive key statistical tasks.
• Develop SAP/AAR, coordinate reviews and ensure QC of methodologies.
• Collaborate on risk assessment, protocol input, and study setup.

Conoscenze

Central Monitoring

Clinical Data Management

Clinical Development

Cross-Functional Teamwork

Data Analysis

Data Governance

Decision Making

Formazione

Master Degree in Statistics, Mathematics, Epidemiology or equivalent

PhD in Statistics, Mathematics or Epidemiology or equivalent

Strumenti

R

Statistical software

Descrizione del lavoro

GSK in Siena, Italy is seeking a Principal Statistician to provide statistical leadership across study designs. You will influence protocol inputs, adaptive design considerations, and decision-making activities within multidisciplinary teams.

Qualifications include a Master’s or PhD in statistics or epidemiology and significant experience with R and clinical trial statistics. Fluency in English is required; Italian language skills are preferred.