CLINICAL SAS PROGRAMMER W/ MASTER'S IN STATISTICS REQUIREMENT #12-00473 RECRUITER: MICHELLE ASHEN JOB LOCATION: HOPEWELL, NJ JULY 25, 2012 Project Description: 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. Master's in Statistics and 9 years of experience are required. Required Skills: Clinical SAS Programming, Master's in Statistics This 12+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Michelle: [Click Here to Email Your Resumé] Requirements Clinical SAS Programming, Master’s in Statistics