Job Description
Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget. One of our clients in Montville, NJ is looking for a Data Management SAS Programmer. This is a contract position.
Responsibilities:
* Ensure in conjunction with (project) data managers, adherence to internal Company standards and validation of all study related calculation and mapping.
* Full responsibilities for data exchange with external parties, for example, CROs, external data providers (Labs, ECG, etc.) and Data Monitoring Committees.
* Setup of Data Management tools for study conduct (edit checks, validity tools, coding, SAE reconciliation, etc.)
* Develop programs for transformation of data from EDC to internal standards. Knowledge of SDTM is a plus.
* Setup of the clinical study database in close cooperation with the EDC database developer and study data manager.
Five plus (5+) years of SAS experience in the Pharmaceutical Industry.
Job Requirements
Five plus (5+) years of SAS experience in the Pharmaceutical Industry.
It is very important that candidates have data management experience. All others may not be considered.
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