*HI All, Please let me know if you have any one for below position.
Job Title : Senior Clinical SAS Programmer Location : Wayne, PA. Duration : 6 Months* *Job Description:* *The Senior 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. As a project lead the Senior Clinical SAS Programmer will provide direction and oversight to programmers in creating sponsor deliverables. * *Based in our Wayne, PA office, the Senior Clinical Programmer's primary responsibilities will include the following: Act as lead programmer to write SAS programs that produce analysis datasets and analyses specified 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 Mentor others in programming and program coding 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 Perform programming in support of sponsor ad hoc requests Produce special reports to comply with regulatory requests May interact directly with sponsors to facilitate project completion The successful candidate will have a combination of the following skills/experience: Minimum 6 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries 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 of SDTM, ADaM, 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 Communicate and collaborate effectively with cross-functional teams in face-to-face conversation, by telephone, and by email Thanks & Regards, Tanvir 201-255-0319 x 293 Email: [EMAIL PROTECTED] * --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Oracle-Financials" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.com/group/Oracle-Financials -~----------~----~----~----~------~----~------~--~---
