Description
This is an exciting opportunity at a successful pharmaceutical firm. As a Principal Statistical Programmer, responsibilities will include, but not be limited to:Project management programming activities on clinical trials studies
Approval of key study-related documents produced by other functions
Collaborative work with multiple departments, including Data Management, Clinical Operations
Excellent personal and written communication skills and ability to present projects in front of
regulatory bodies and upper management
Ability to communicate highly complex/technical information clearly to colleagues across departments
and from varied backgrounds
Attend external professional organizations, conferences, training, or meetings
Competitive candidates will be comfortable with CDISC, STDM, and the SAS System version 9.1.3. Also will have a good understanding of computer operating system, including UNIX.
Education:
Masters preferred
Bachelor's with 5 years experience in relevant field
To find out more about Real please visit www.realstaffing.com