Senior Biostatistician (Switzerland)

Responsibilities include, but are not limited to:

• Post-hoc statistical analyses to support International regulatory filings, publication planning and health economic analyses
• Provide face-to-face statistical input for projects to which he is assigned
• Provide statistical input into the design of protocols including preparation of the biostatistical analysis section.
• Prepare statistical analysis plans including table shells.
• Analyze and report results of clinical trials. Provide tables, listings and graphs for final study reports
• Manage outside CROs and consultants Skills/Knowledge Required:
• Master’s Degree/Ph.D. in statistics with focus on statistical methods appropriate for clinical trial
• Demonstrated skills and experience in a statistical department including direct interaction with clinical personnel in the planning, analysis and reporting of clinical trials either in a pharmaceutical industry or similar academic setting
• Experience with working on an NDA or sNDA is desirable, but not required
• Detailed knowledge of statistical regulatory requirements
• Excellent SAS skills including report generation
• Knowledge of MS Office products (Word, Excel)
• Experience in oncology trials would be an asset
• Excellent interpersonal, communication, writing and organizational skills
• Demonstrated ability to work in a team environment with medical personnel, clinical monitors, data managers, programmers and medical writers

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