Hi All,


Hope you are doing well!!!!


Please Send me the suitable profiles to sop...@datagrp.com for the below 
mentioned requirement with rate confirmation.

Position: SAS Statistical Consultant
Location: Sunnyvale, CA
Duration: 6 Months Contract

Rate: $40/hr (Not Negotiable)


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 

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,

Sophia Jones
Technical Recruiter
Data Group, Inc.
Certified Minority Women Owned Business Enterprise (MWBE) & Small Business 
Enterprise (SBE)
|Office: 1 - 732 - 791 - 2348 xtn: 250| Fax: 732 - 907 - 1174 |Email: 
sop...@datagroupinc.net|Website: www.datagroupinc.net|
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