Statistical Programmer

The candidate will be responsible for:
• Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions.
• Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead.
• Able to support multiple protocols independently and to contribute to integrated summaries of efficacy and safety.
• Demonstrates strong SAS programming skills; participates in protocol team and some project team interactions.
• Builds successful relationships and seamless interfaces at the protocol/project team level.
• Provides timely and effective communication to the programming and statistics leads.

Required: 
• BS degree Statistics
• 7-9 years of Statistical Programming experience within the pharmaceutical industry

Desired:  Advanced degree preferred.