• Responsible for providing statistical and programming support to Clinical Operations and/or Medical Affair projects
• Participate in the development of study protocols including participation in study design discussions and running scenarios and modeling to determine the best strategy for Phase 3b/Phase 4 studies
• Review CRFs and data edits
• Develop Statistical Analysis Plans including analysis files and report/programming specifications
• Perform statistical analyses including the production of Tables, Figures and Listings , interpreting statistical results and helps prepare study reports for presentations and publications
• Responsible for managing project related analysis and programming execution performed by junior staff members and/or Contract Research Organizations
• Provide input into the development of biostatistical and data management SOPs, work instructions, and analysis macro programs.
• Assist Business Development in supporting joint analyses with partners, evaluating in-licensing and out-licensing opportunities

Qualifications:

Must be able to exercise judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.

Computer Skills:
SAS Programming and MS Office.
Other Skills and Abilities:

Excellent written and oral communications.

M.S. or Phd. degree in Biostatistics, Statistics or Applied Mathematics