Send resumes to j...@technogsolutions.com or reach me *404-537-9593.* *Role: SAS Programmer* Loc: Hamilton, NJ Duration: 12 months NOTE: Only GC-EAD, GC and US Citizens please (*No H1b/OPTs*)
*Job Description: * Senior SAS computer programming position working with clinical trials data. Primary responsibilities include providing clinical data management and biostatistical programming support for various phases of clinical studies. Activities include importing/exporting data, reformatting raw data to CDISC (SDTM & ADaM) and/or client specified analysis standards, programming and/or validating analysis data sets, tables, listings, graphs, ad hoc reports and regulatory submission deliverables such as ISS, ISE, and eCRT and Define documents. Assists Data Management and Biostatistics with developing tools and techniques for improving process efficiencies. Communicates effectively within a multi-disciplinary project team to complete assigned tasks on time and within budget. Resolves issue escalation for lower level programmers. Reviews and makes recommendations for process development and improvement. *Statistical Programmer Contractor Key Responsibilities: * •Provide statistical programming support as well as operational guidance and coordination for assigned projects and act as a project statistical programmer with the advice of teams; •Support the preparation of clinical trial reports and, if necessary, integrated summaries of effectiveness and safety, using appropriate statistical, and clinical trial methodologies, and computer applications; •Perform QC of tables and programs developed or produced by Teams or by Clinical Research Organization (CRO) personnel; •Performs exploratory analyses of data; •Actively participate in preparation of abstracts/presentations/manuscripts based on clinical study data and interact with members of teams, Marketing, DRA, Medical Data Management, Biometrics, and Medical and Scientific Affairs personnel to accomplish the major job objectives. and •Interact with CROs to ensure efficiency and quality in completion of statistical activities contracted out for assigned clinical trials. •Participate in: o the development of project plans, protocol design and development o the development of trial validation plans and source data verification plans o the preparation of documents needed for Reporting and Analysis meetings (table/figure/listing shells and programming specifications). o the preparation of abstracts/presentations/manuscripts •Prepare: o statistical mock up tables of protocols which will be approved by the project statistician or group head o statistical files/programs for submission to health authorities, if necessary o statistical programming sections of clinical trial reports which meet the statistical guidelines of the departments and health authorities •Review CRFs for soundness of trial design and discuss comments directly with clinical research personnel/project statistician/group head •Review and attend Protocol Review Committee meetings when necessary •Review and approve statistical program deliverables prepared by external groups •Provide guidance in the preparation of data listings, summary tables, graphs and statistical analysis files. •Manage activities related to data analysis, report preparation, transfer of data to and from CRO, and archiving of clinical trial data, output and programs following processes •Perform QC of the tables and programs developed by other statisticians and programmers •Perform exploratory analysis of data •Any other related tasks as directed by supervisor -- You received this message because you are subscribed to the Google Groups "Exact Match" group. To unsubscribe from this group and stop receiving emails from it, send an email to exact-match+unsubscr...@googlegroups.com. To post to this group, send email to exact-match@googlegroups.com. Visit this group at http://groups.google.com/group/exact-match. For more options, visit https://groups.google.com/d/optout.
