Statistical Programming Contractor Location: San Francisco, CA
This is a 6-12month contract with a rate between 50-60p/hr depending on experience. Oncology and strong CDISC experience are a must. *WOULD REQUIRE F2F AFTER PHONE SCREEN !!!!* The Statistical Programming Contractor will work in XXXXXX Statistical Programming group in the Oncology Therapeutic area. This position will report to Sr. Manager, Statistical programming within the Biometrics group. *Responsibilities:* *>* Assist in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans and other clinical documents *>* Write, test and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications *>* Write CDSIC standard dataset specifications and follow specifications to create SDTM and ADAM datasets *>* Understand and execute department-, product- and study-level macros and utilities. *>* Write, test and validate product- and study-level macros and utilities *>* Provide input to and participate in intra-departmental meetings *>* Contribute to the continuous improvement of Statistical programming group *>* Assist in the review of Statistical Programming policies, standard operating procedures and other controlled documents *>* Provide support to and mentor junior programmers and contractors *>* Interface with outsourcing partners and vendors *>* Attend external professional organizations, conferences, training and/or meetings *Knowledge: * Computer programming, SAS or other procedural languages Understanding of computer operating systems, word processors, document applications Fundamentals of project planning and management Drug development process *Preferred Qualifications:* Bachelors or Master’s degree, in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject 6 years clinical research and development programming experience Extensive hands-on experience in developing CDSIC standard specifications and datasets (SDTM, ADAM) Experience in Oncology Trials Experience in FDA/EMEA trial submissions Drug Development (pre-, early, late and/or observational) in related industries or academic research *Regards Alex Page* -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To post to this group, send email to citrix-and-sap-probl...@googlegroups.com. To unsubscribe from this group, send email to citrix-and-sap-problems+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/citrix-and-sap-problems?hl=en.
