Hi Partners, Kindly let me know if you have any consultant for the following position.
* * *Please respond back with an updated resume and all inclusive rates to recrui...@burgeonits.com* *Position: Sr. Clinical SAS Programmer * *Location: WAYNE PA * *Duration: 12 months * * * *Basis Qualifications- * · *Minimum of a Bachelor’s degree * · *Minimum 6 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries.* * * *Preferred Skills * · Extensive knowledge of Base SAS, SAS/GRAPH, SAS/STAT, and ODS · Experience working with heterogeneous data structures · Ability to work independently and adept at managing multiple competing tasks · Good understanding of clinical data and pharmaceutical development · Knowledge and experience using SDTM and Adam, data structures · Knowledge of FDA and ICH guidance · Knowledge of clinical trial conduct and the data and reporting requirements for clinical trials · Knowledge of SAS programming techniques needed to produce outputs in accordance with specifications The Clinical SAS Programmer creates SAS programs in support of sponsor’s clinical trials according to SOPs and guidelines. This programmer will create, document, validate, process, and maintain statistical programs and macros that generate analysis datasets, tables and graphics with high quality per agreed timelines. For the project lead position, the Clinical SAS Programmer will provide direction and oversight to programmers in creating sponsor deliverables. · Act as lead programmer to write SAS programs that produce analysis datasets (ADaM) and analyses specified (ADaM) in the Statistical Analysis Plan · Act as quality control programmer to validate SAS programs that produce analysis datasets and analyses specified in the Statistical Analysis Plan · Assist the Manager of Clinical programming in overseeing the daily tasks associated with clinical programming and subsequent analysis to ensure sponsor deliverables are created per agreed timelines and to high quality standards. · Ensure SAS programs adhere to SOPs, guidelines, and specifications · Ensure SAS program output matches the requirements of the Statistical Analysis Plan · Consult with managerial, statistical, data management, DIS, and medical writing personnel to clarify program intent, identify problems, and suggest changes. · Design and/or review database structure · Create derived-analysis datasets · Execute analyses specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plan (RAP) under the guidance of the project statistician · Take instructions and perform tasks as necessary as directed by reporting manager · Ensure specifications and documentation are correct and complete · Work with other team members to ensure outputs are correct and complete · Organize, plan, and prioritize work to develop specific goals and plans to prioritize, organize, and accomplish project objectives · Analyze information and evaluate results to choose the best solution and solve problems. * * *Note: Client is not accepting profiles who worked with Pfizer, Celegene, Baxter, Johnson & Johnson before*** Thanks & Regards *Raja* Burgeon IT Services LLC Ph: 302-220-4724 FAX: 302-355-1559 Email: recrui...@burgeonits.com Website: www.burgeonits.com NOTE: We respect your Online Privacy. This is not an unsolicited mail. If you are not interested in receiving our E-mails then please reply with a "REMOVE" in the subject line and mention all the E-mail addresses to be removed with any E-mail addresses which might be diverting the E-mails to you. We apologize for any unintended inconvenience. -- You received this message because you are subscribed to the Google Groups "CorptoCorp" group. To unsubscribe from this group and stop receiving emails from it, send an email to corptocorp+unsubscr...@googlegroups.com. To post to this group, send email to corptocorp@googlegroups.com. Visit this group at http://groups.google.com/group/corptocorp. For more options, visit https://groups.google.com/groups/opt_out.
