Hi, Please send suitable profiles along with rate and contact info. ** *Req #1:*
Position Title: Clinical Stats Programmer Location: Livingston, NJ Experience: 3 + Yrs Duration: 6+ months Positions: 2 *Job Description*: Our client, a leading pharmaceutical company, is looking for two Contract SAS Programmer. They need statistical Programmer who will provide high quality work in support of our clinical studies. *Responsibilities*: Evaluate programming tasks needed for clinical studies or NDA submissions. Assist Bio statisticians in design and setup of mock summary tables, listings, and figures pertaining to safety and other parameters as required. Create or modify SAS programs to generate the appropriate tables, listings, and figures involved in the aforementioned activities and to prepare documentation of all programs written. Assist in the design of specific or integrated SAS databases. Participate in the design and writing of global standard SAS programs. Coordinate and guide the programming activities of on-site program consultants and/or off site CROs; audit work as required. You will have a coordinated work schedule to fit project requirements and time lines while at the same time working independently with minimal supervision *Qualifications*: Bachelor's degree in Biostatistics, Statistics, Computer Science. Three to five (3-5) years of pharmaceutical industry experience in SAS programming. Experience in data analytic concepts, logically analyze programming requirements, *Req #2:* Position Title: *SAS Programmer* Location: Cambridge, MA Duration: 6+ months(Long Term) *The Statistical Programmer will be responsible for:* - Writing and testing SAS programs from instructions provided by Biostatisticians and Statistical Programmers to create tables, figures, and listings reporting the results of clinical trials for investigational medications - Performing quality control checks of SAS code and output - Compliance with FDA/ICH/GCP regulations - Application of good working knowledge of medical data, the design and phases of clinical trials, statistics, relevant GCP/ICH/FDA regulatory requirements, and the pharmaceutical industry to the execution of all tasks Qualifications: Qualified Candidates should posses: - B.S. in Biostatistics, Statistics, Computer Science, or a related field - A minimum of 5 years of SAS and relevant pharmaceutical industry experience. - Experience with writing SAS programs from instructions - Experience with all SAS language, procedures, and options commonly used in clinical trial reporting - Experience working with all types of safety data and coding dictionaries (MedDRA and WHODRL) *Thanks & Regards,*** *Jitha Radhakrishnan*** *Vaptech Inc.*** 1001 Durham Ave, Suite 200, South Plainfield, NJ 07080 [EMAIL PROTECTED] *Voice: 732-767-0700 *3003* Fax No - 732-767-9669 Disclaimer: This is not meant to be an unsolicited email, So If you want to be removed, please send mail with *REMOVE* in the *Subject* & I will promptly remove upon receipt. --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "zilliontechnologies" group. To post to this group, send email to zilliontechnologies@googlegroups.com To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.com/group/zilliontechnologies?hl=en -~----------~----~----~----~------~----~------~--~---
