*New Contract Opportunity Contract Clinical SAS Programmer Major Pharmaceutical 12 Month Contract Berkeley Heights, NJ*
*Contract Clinical SAS Programmer* *Responsibilities*: 1. Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. 2. Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. 3. Perform ad hoc flexible and rapid programming arising from questions generated from planned analyses and results. 4. Ensure consistency and adherence to standards within their therapeutic area. 5. Provide programming support for the preparation of integrated reports, submissions and post-submission activities. 6. Oversee the services provided by CROs. 7. Contribute to the creation, maintenance, and validation of standards for programming tools, outputs and macros. 8. Provide training on departmental SOPs/WPs and standard programs. 9. Contribute to the creation of naming conventions and standards for the programming environment. 10. Participate in industry wide technical discussions. * Required: *• Bachelor’s degree in life science, statistics, mathematics, computer science, or related field is required; Master’s degree is preferred. • 6 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions with a Bachelor’s degree; or 5 plus years experience with a MS/MA degree. • Demonstrated proficiency in using SAS to produce derived analysis datasets and produce TFLs. • Thorough understanding of clinical data structures, relational database structures, and data exchange with alternate data formats. • Demonstrated skills in using additional software tools and applications (e.g. MS office, XML). • Demonstrated expertise in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM. • Demonstrated expertise in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission. • In-depth understanding of regulatory, industry, and technology standards and requirements. • Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs. • Demonstrated ability to work in a team environment with clinical team members. • Good interpersonal, communication, writing and organizational skills. *Contract Clinical SAS Programmer* -- 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 http://groups.google.com/group/sap-or-oracle-financials. For more options, visit https://groups.google.com/d/optout.
