BIOSTATISTICS

Contribute to the development of protocol

Develop Statistical Analysis Plan (SAP)

Analyze data

Develop Tables and Listings for Clinical Trial Report 

Provide On-going Biostatistical Support 

• Attend team meetings 

• Advice on biostatistics topics

• Attend meetings with partners

• Produce materials for investors or

     business development presentations

Contribute to all Clinical Study Documentation(integrated,ICH standard) including appendices

Develop Protocols, Synopses, and Appendices

Develop Informed Consent Forms

Prepare Clinical Study Reports (Phase I - IV)

Create Patient Materials to increase compliance and recruitment/retention

Develop SOPs, Work Instructions, Forms and Templates