Biostatistician

Description The Biostatistician will be responsible for the following duties, among others:
• Provides input on design of studies and reviews protocols
• Computes sample sizes in conjunction with clinical staff as required for clinical studies
• Writes detailed analysis plans and analyzes clinical data, as directed by immediate supervisor
• Designs summary tables, reports, and graphs for presentation of results
• Writes statistical analysis descriptions for protocols and final reports, as directed by immediate supervisor
• Consults with others in company on statistical issues when requested
• Creates and modifies, or directs the creation and modification of SAS programs to support all of the above
• Maintaining statistical and programming activities and documentation in accordance with Company's policies, procedures and all standard operating procedures (SOPs)
• Maintaining thorough knowledge of all Company systems, utilities and other tools

Requirements • Masters or PhD in biostatistics or statistics is required
• At least 5 years of pharmaceutical industry experience with Masters Degree; at least 3 years of pharmaceutical industry experience with PhD