SAS^® Programming

Chastain Research Group, Inc.

SAS^® Programming services

We need experienced SAS^® statistical programmers providing on-site and off-site programming support for clinical trial research (Phases I-IV) and filings like New Drug Applications (NDAs), Biologic Licensing Applications (BLAs), investigational new drug (IND) updates, medical device pre-market applications (PMAs), exemption requests for investigational devices (IDEs) and 510(k) pre-market notifications. Ability and experience with clinical trial data including data edit checks, data specifications (CDISC), statistical analysis procedures, standard operating procedures (SOPs) and following statistical analysis plans (SAPs) for producing FDA quality tables, listings and graphs (TLGs) along with Case Report Tabulations.

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For further information: e-mail chastain@chastain.com, call us at 1-650-566-8066 or fax us at 1-800-407-2528.

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