Hi,

 

Location: Boston (Only Locals)

Duration: 6+ Months

Rate: $55/hr

 

Our client has an immediate opening for a Clinical SAS Programmer who has 7
years of experience supporting Phase II/III Clinical Trials in a
Pharmaceuticals.

Duties: 

- Provide statistical programming expertise (preferably in SAS) in the
production of analyses, tabulations, graphics, adhoc requests and listings
from clinical trial data. 

Key responsibilities and skills include, but are not limited to, the

following: 

* Contribute to the preparation of analysis plans. 

*Prepare, document and test required programs and procedure data displays in
an efficient manner for inclusion in integrated clinical, statistical
reports and other similar reports. 

* Contribute to the integrated clinical/statistical report and other similar
documents. 

* Ensure analysis data and programming code meet regulatory and company
standards and are consistently structured to permit efficient programming
and reporting. *Perform quality assurance procedures on work performed by
others. 

* Develop, test, validate, document, maintain and execute software and/or
systems using the currently endorsed tools or support of production
activities. 

Knowledge with Datacutics reporting tool is preferrable.

Required Skills: 

Understands the basic skills and goals of reporting clinical data. Writing
knowledge of SAS and SQL. Proven ability to organize workload and priorities
and complete tasks on time. Demonstrated ability to work effectively in a
team environment. Strong interpersonal skills and ability to communicate
effectively. Ability to identify and solve technical problems

Education: Advanced degree in Science or Mathematics

 

 

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Thanks & Regards,

Rajesh 

Simplex Info Systems, Inc.

Wellington-FL

Ph.No: 561-273-1131

Fax  : 603-386-6244

Email: [email protected] 

Y! messenger :  rajesh.simplexinfo 

www.simplexinfo.com <http://www.simplexinfo.com/>  

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