Description
New Contract Opportunity!!Sr. Clinical SAS Programmer
Contract Research Organization
Central New Jersey
Rate is Open
Description:
Design, develop, and validate SAS programs for the generation of data tables, listings, and figures for clinical study reports, and integrated analyses.
Responsibilities:
- Design, develop, and validate SAS programs for creation of standard datasets.
- Develop data transfer specifications for external data transfers.
- Interact, as needed, with external data vendors.
- Trouble shoot problems with clinical datasets.
- Evaluate data, results and/or document findings; interact with other programmers and departments to provide and recommend solutions on clinical programming and/or clinical data issues.
- Provide direction to other clinical programming employees. Receive no instruction on routine assignments and minimal instruction on new assignments.
MUST HAVE:
- Bachelors degree in mathematics, statistics, or equivalent.
- 6+ years of Clinical Programming experience in a Pharmaceutical/CRO or Equivalent
- Ability to effectively motivate and direct the activities of others.
- NDA submission experience, including ISS programming and submission dataset development within current industry data submission standards.Call or email me if you have any questions. Contact details are on my Linkedin Profile. Search for Paul Dai
Thanks
Paul Dai
To find out more about Real please visit www.realstaffing.com