*Send resumes to a...@datagrp.com* * *
*Position: SAS Statistical Consultant Location: Sunnyvale, CA Duration: 6 Months Contract* *Rate: $40/hr (Not Negotiable)* *JOB DESCRIPTION:* *Job Duties:* Uses a variety of statistical methods and software tools to analyze and display data. Methods must be appropriate for the kind of data collected, and required assumptions must be tested., Interprets statistical findings, and ensures that regulatory submissions, reports, and manuscripts accurately reflect the data collected., Validates and provides clear documentation of analysis programs., Consults with colleagues on statistical and analysis issues., Writes the statistical analysis plan for the study. Writes error-checking requirements for the study data. Applies statistical knowledge to the design of clinical studies. This requires calculation of sample size and power, as well as solicitation of appropriate design assumptions from other staff and from published literature. Prepares relevant sections of protocols, especially those detailing the plans for data analysis, and justification for the sample size. Assists study teams in responding to questions from FDA. Attends and contributes to project and department meetings., Perform statistical program validation in accordance with departmental Standard Operating Procedures., Manage multiple, varying sized projects concurrently., Participate in development and documentation of study protocols with responsibility for scientific soundness sections, which include statistical hypotheses, sample size calculations, and analysis methods for meeting the study objectives, in collaboration., Develop statistical programs (e.g., using SAS, S-PLUS, R, WinBUGS) for data extraction, statistical analysis, and report generation. *Request Notes: * Title: Statistics Consultant/Senior Statisticians PhD in statistics or biostatistics from an accredited college or university and a minimum of eight (8) years experience in a clinical research/medical setting required. Prior experience in interfacing with FDA and advisory panels is essential. Experience in orthopedic (especially spinal) and device-biologic combinational devices is preferred but not required 1. Develop and review clinical studies Statistical Analysis Plans (SAPs). 2. Be able to provide Statistics consultation which includes using Advance Statistical Models, e.g Propensity Scores Analysis 3. Ensure that table shells/listings are programmed according to the SAP. 4. Provide statistical support for company's Health Economics, and provide input to data analysis used for publications directing analytic and statistical executions; interpreting results; authoring methodological and statistical sections of manuscripts; reviewing and approving abstracts, presentations, manuscripts, and other study reports; and ensuring high quality of publications. 5. Attend and participate in Clinical Data Management, Statistics, and project teams meetings as needed (for statistical input) 6. Provide statistical input to clinical studies as required. This will include Study design and sample size estimations. 7. Provide statistical input for requests initiated by Data Safety Monitoring Boards (DSMB) as needed. 8. Provide interpretation of statistical outputs produced as needed. Schedule: 10-12 hours a week, (may be less). This person will work remotely except for very few times that he/she may visit the facilities Thanks & Regards, *Alex Rodriguez* *Account Manager* *Data Group, Inc.* * * *Certified Minority Women Owned Business Enterprise (MWBE) & Small Business Enterprise (SBE)* ------------------------------ *|Ph: 732 – 734 – 5343|Office: 1 – 732 – 791 – 2348 xtn: 254| Fax: 732 – 907 – 1174 |Email: a...@datagrp.com | Website: www.datagroupinc.net|* ------------------------------ --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Oracle / Data Warehousing Developers / ETL" group. To post to this group, send email to Oracle-Data-Warehousing-Developers-ETL@googlegroups.com To unsubscribe from this group, send email to oracle-data-warehousing-developers-etl+unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.co.uk/group/Oracle-Data-Warehousing-Developers-ETL?hl=en-GB -~----------~----~----~----~------~----~------~--~---
