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Projektbeschreibung
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 [1]
Links:
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[1] http://www.realstaffing.com
To find out more about Real please visit www.realstaffing.com [1]
Links:
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[1] http://www.realstaffing.com
Projektdetails
Geforderte Qualifikationen
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