CLINICAL SAS PROGRAMMER
Posted: 7/21/2010
Type: Contract
Length: 6 Months
Location: Maryland
Description
Our client is a growing pharmaceutical company that looking to add an experienced SAS programmer to support Data Management
The clinical SAS programmer will be responsible for and not limited to the following activities:
- Program and validate tables and listings that are required for clinical review as assigned gathering requirements from the team or defined in the edit review specifications document
- Program and validate edit checks as specified in the Data Management Validation Plan
- Create, document, validate, and design the SAS programs specified in the Data Management Validation Plan for QC/QA audits or in response to ad-hoc requests
- testing of new databases in Clinical Data Management Systems
Requirements
- BS degree in Statistics or Computer Science
- A minimum of five years of SAS Programming working in clinical trials
- SAS Base and SAS Macro languages, experience using SAS ODS
Preferred:
- Experience with SAS Graph, SAS STAT
- CDMS experience (Clintrial, Oracle Clinical etc)
- EDC experience
- Experience with Government regulations (GCP, ICH)
To apply, please contact:
Email: job@orbisdata.com
