To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

Job #02902

About our client Our client is a leading medical device company specializing in ophthalmology and eye care products. They have over 13,000 employees globally and a reputation as a leading innovator in the field. With operations in 36 countries and a 150-year track record of success, this is a great situation for a candidate pursuing a challenging opportunity with a world-class employer. Position Location Senior Clinical Programmer Analyst New York Salary Highly competitive package, commensurate with experience Responsibilities 1) Develop formal and ad hoc reports for the Pharmacovigilance Group 2) Assist the Global Statistics Group to develop SAS programs for reporting clinical trial results 3) Develop and produce tables as well as listings for statistical and clinical report writing 4) Create/modify SAS programs to carry out the analytic plan 5) Execute (or oversee execution of) the analytic plan for research studies 6) Assess feasibility of analytic plan and timeline associated with analytic plan 7) Investigate issues with the data and report findings back to team 8) Serve as lead analyst on large studies that require more than one analyst to complete the work 9) Document steps taken and validate/crosscheck results 10) Draft and review methods section of reports 11) Serve as technical resource to other analysts 12) Present new programs/techniques and output methods to other analysts 13) Develop ability to mentor new analysts 14) Assist in development and documentation of standard table output methods and programs 15) Provide ad hoc and formal reports for Pharmacovigilance using SAS, PL/SQL or other suitable reporting tools and standardizing reports (as appropriate) 16) Execute SAS programming and other software packages (as necessary) 17) Perform analyses for regulatory and marketing studies, including development of standard programs within the Statistics Group 18) Communicate with data management, clinical personnel and medical writers on data quality questions, CRF review (and annotations), editing checks and clarifications of analysis strategies for new parameters 19) Check statistical and data tables, listings and figures (generated internally and externally) to validate consistency of information presented and results from independent programmers Requirements 1) BA/BS in Computer Science, Mathematics or a related field 2) 4+ years of experience in SAS programming with knowledge of and experience in clinical trials 3) 2+ years of experience as a SAS programmer/analyst for a drug/device company or CRO 4) Proficient in Base SAS and other SAS reporting modules 5) Expertise in SAS macros and SAS STAT/GRAPH preferred 6) In-depth knowledge of relational database theory, Base SAS, SAS Graph, SAS Stat and SAS Macros 7) Understanding of medical terminology, physiology, anatomy and standardized medical coding dictionaries a plus 8) Familiarity with transaction-based processing in Oracle, SAS Data Null, SAS Proc SQL, SAS Proc Report, ODS and SAS Arrays a plus 9) Understanding of medical terms associated with the eye an asset 10) Excellent organizational and communication (verbal and written) skills