DUTIES – RESPONSIBILITIES:
The Clinical Data Manager (CDM) will be responsible for all data management activities from study start up to database lock. The CDM will work on studies independently or will manage CROs & interact with outside vendors. The CDM will perform medical dictionary coding. The CDM is also responsible for creating databases and providing programming support as required.
Sigma Bullhorn ID: 7127
Position/Role: Senior Scientist
Location(s): Pearl River Area, NY
Client Industry: Biotechnology/Pharmaceuticals
Classification: 10 Months Contract (Extension Likely Into Second Half of 2016 or Conversion to FTP Status)
PLEASE NOTE: Remote Work is NOT allowed. On-Site Only. If you have any questions, I’ll be happy to answer them, but I’ll need to see a copy of ...
Are you a CRA with less than 1 year of monitoring experience OR a nurse or study coordinator with an oncology background that is looking to use your skills in a whole new way?
If so, it's your time to SHINE at Covance!
Covance is a leading supplier of drug development services to the biotechnology and pharmaceutical industries. We partner with innovative companies, offering valuable ...
The Programmer/Analyst II uses statistical software (SAS, SPSS etc.) and works under general supervision to generate analysis data sets, tables, listings, and figures as well as results for any post-hoc analyses. This individual is responsible for assisting with the oversight of all CRO data management and programming aspects ensuring the data management and programming performance ...
May 6 -
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