Description
Clincial SAS Programmer-Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions.
-Assume 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.
-Build successful relationships and seamless interfaces at the protocol / project team level. Provide timely and effective communication to the programming and statistics leads.
Required Skills:
- MS in Statistics, Biostatistics, Computer Science or related field
- 7 - 9 years' experience
To find out more about Real please visit www.realstaffing.com