A new Job, ID: 133039 <http://ejobsville.com/display-job/133039> was added at eJobsVille.com - For the Best Tech Jobs in Town <http://ejobsville.com>
Title: Clinical Sas Programmer (GC's & Citizen's) Local To NJ posted on 2014-03-20 08:02:57 Job Description:Hi, We are looking for *Statistical Programmer *in *NJ* kindly go through the below job opening and let me know your interest. Please send resume in word format along with pay rate details. *Job Title: Statistical Programmer* *Location: East Hanover,NJDuration: 6 Months Extendable ContractClient: Novartis * *Duties: * *Candidate should be able to perform development of analysis datasets, generation of tables, listings and graphs from both internal and external data sources. Must be able to demonstrate experience in generation preparation of analysis dataset, generation of both safety and efficacy tables, listings and graphs and strong validation skills. Ideal candidates should be able to demonstrate clinical trial data flow, especially in Oncology. Previous pharmaceutical SAS experience is mandatory. Minimum of 3+ years previous SAS programming and development. Consultant will be working with existing code and modifying or adding to it. Will be working in a team environment with multiple programmers. S/he develops and complies with project/study standards and specification s following internal and regulatory guidelines. S/he maintains records for all assigned projects and archives trial/project analysis and associated documentation. Clinical pharmacological trial experience is preferred but not required.* *Skills: * *Expert knowledge/experience in SAS software. Good knowledge or drug development process. Excellent verbal and written communication skills. Good organizational interpersonal and diplomacy skills. Continuous improvement mentality and attention to detail. Intermediate knowledge of Office tools* *Candidate should be able to perform development of analysis datasets, generation of tables, listings and graphs from both internal and external data sources. Must be able to demonstrate experience in generation preparation of analysis dataset, generation of both safety and efficacy tables, listings and graphs and strong validation skills. Ideal candidates should be able to demonstrate clinical trial data flow, especially in Oncology. Previous pharmaceutical SAS experience is mandatory. Minimum of 3+ years previous SAS programming and development. Consultant will be working with existing code and modifying or adding to it. Will be working in a team environment with multiple programmers. S/he develops and complies with project/study standards and specification s following internal and regulatory guidelines. S/he maintains records for all assigned projects and archives trial/project analysis and associated documentation. Clinical pharmacological trial experience is preferred but not required.* *SAS* *Education: * *Minimum of BA/BS or equivalent education/experience in mathematics, statistics, computer science or life science or related field(s). Expert knowledge/experience in SAS software. Good knowledge or drug development process. Excellent verbal and written communication skills. Good organizational interpersonal and diplomacy skills. Continuous improvement mentality and attention to detail. Intermediate knowledge of Office tools.* *BA/BS* Salary: 50 *Click here to view full job description and apply <http://ejobsville.com/display-job/133039> (Registration not mandatory to apply for this job)* ------------------------------ Best regards, eJobsVille.com - For The Best Tech Jobs In Town Best regards, eJobsVille.com - For The Best Tech Jobs In Town -- You received this message because you are subscribed to the Google Groups "SAP ABAP" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/sap-abap. For more options, visit https://groups.google.com/d/optout.
