Hi,

Hope you are doing great!!!

Please let me know if you have any consultant for the following requirement.




Send Resumes to [email protected]



Position: Sr. SAS Statistical Programmer

Location: Ridgefield Park, NJ

Duration: 6+ months

Must be local



*Description: *

Provide statistical programming and validation support for clinical studies,
including overseeing and validating programming activities by external
vendors (e.g., CROs)

· Provide programming supports for publication and marketing strategies,
work closely with manager of programming to generate and QC outputs for
publications; review publication (abstract/manuscripts) to ensure accuracy,
quality and soundness of statistical methodologies.



Work with the clinical study team on study design, development and/or review
of clinical study protocols, statistical analysis plans and final study
report; perform post-hoc statistical analyses as needed.

· May work with the Health Outcome team on the design/analysis/validation of
projects.



Develop dataset specifications, provide input to database and CRF
development, create edit check programs and listing generation macros for
Data Management.



*Qualifications: *

At lest 5 years experience in SAS programming for Phase I-IV clinical trials
in pharmaceutical/CRO environment.

Bachelor's degree in Statistics or a related science discipline (Master or
PhD in Statistics preferred).

Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS office.

Experience with Unix and Windows operating systems.

Understanding FDA guidelines.

Some experience in CDASH and SDTM is a plus.





Thanks & Regards

Adem
Technical Recruiter
Vertigon Consulting
Phone: 201-402-1610
Fax: 732-398-0506
Email: [email protected]
URL: www.vertigonconsulting.com

IM:  [email protected]

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