12 month contract with a large pharmaceutical company. This contract is extendable as the current group has pipeline for at least 24 months.
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.
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.
Provide timely and effective communication to the programming and statistics leads.
MS in Statistics or related field is preferred; BS with 6+ years
Minimum 5 years SAS experience in Pharmaceuticals or related fieldTo find out more about Real please visit www.realstaffing.com
Real - 20 months ago