Hello Partners,
Hope you are doing great, *Seeking SAS Programmers for a long term contract role with client in Woodcliff Lake, NJ. * *EAD GC, GC or USC - LOCAL to NJ or PA who can do Inperson Interview, VISA Copies MUST be Provided with submission.* *Duration: 12+ months Contract* *Interview process: Phone, then face to face. NO SKYPE INTERVIEWS! * Support the Biostatistics team by carrying out and conducting programming activities of statistical programmers, and coordinating with external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. *Main duties/responsibilities: * Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: analysis datasets, statistical tables, figures, listings, Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy (ISE), DSUR, PSUR, IB, progress reports, electronic submissions and other internal and external requests (e.g., publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors in order to develop or monitor the content and structure of SAS data sets. *Strong technical skills and Oncology experiences supporting submissions are required. * *Strength in ADaM datasets are critical* *Experience required: * - Minimum 3 years’ experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. 6+ years’ experience preferred. - Some project experience in a pharmaceutical programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical environment. - Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. - *Knowledge of SDTM and ADaM standards. Strength in ADaM datasets are critical* - Proven experience with UNIX and Windows operating systems. - Understanding of the software development life cycle. - Understanding of FDA guidelines. - Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. - Applies good judgment and demonstrates initiative to resolve issues. - Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment, managing that team as required *Minimum of Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related science discipline.* *Strength in ADaM datasets are critical* *MORE PHARMA INDUSTRY NOT CRO.* *Strong technical skills and Oncology experiences supporting submissions are required. * *Knowledge of SDTM and ADaM standards*. Regards: Sam Williams - Recruiting Manager ITBrainiac Inc. Direct : 646-499-5264|| Fax : Fax 312.582.2699 116 Village Blvd, Suite 200 - Princeton, NJ 08540 swilli...@itbtalent.com || swilli...@itbrainiac.com www.itbrainiac.com -- You received this message because you are subscribed to the Google Groups "SAP or Oracle Financials" group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-or-oracle-financials+unsubscr...@googlegroups.com. To post to this group, send email to sap-or-oracle-financials@googlegroups.com. Visit this group at https://groups.google.com/group/sap-or-oracle-financials. For more options, visit https://groups.google.com/d/optout.
