*Good Afternoon Friends *

 *We Request You To Provide The Top Qualified Profiles For This Requirement*


*Position : SAS Developer*

*Duration: 6 Months +*

*Location : Location: Nashville, TN*

*Knowledge & Skills *

*Hands-on experience and knowledge with SAS and other statistical software
along with SDTM and Macro programming.*

*Good knowledge in applied statistics including study design methodologies,
categorical data analysis, survival analysis etc. *

*Exposure to the use of modeling and simulation to enhance clinical trial
design and decision making would be advantageous.*

*Good understanding of clinical research and drug development process, and
requirements on  regulatory submissions and compliance*

*Familiar with ICH guidelines, regulatory requirements and industry
standards (eg CDISC) and awareness of best practices related to statistical
and programming activities*

*Excellent verbal and written communication skills and presentation skills
Patient / Customer-focused*


*Represent biostatistics department on project teams, provide support and
guidance on data and statistical-related issues to the teams *

Provide statistical input and support related to trial design and in the
development of protocol synopses, protocols and *CRFs.*

Advise Data Management with respect to database design, validation checks &
key data, to ensure that all data required for analysis purposes are
captured adequately
Develop randomization schema


*Develop statistical analysis plans (SAP)*

Perform data review to ensure data are suitable for analysis

Work with the programmers to provide definitions, specifications,
documentations and review of derived datasets required to produce the
planned statistical outputs, including tables, figures and listings

Produce statistical outputs for various analysis and reporting purposes,
and provide statistical review and program validation for each project, to
ensure the integrity, adequacy and accuracy of the outputs.

Provide statistical insight in the interpretation and discussion of study
results, and provide statistical contribution to the integrated clinical
study reports and publications
Maintain professional statistical standards by keeping abreast of new
developments in statistics, drug development and regulatory guidance
through literature review and attendance/participation at workshops and
professional meetings

*Understand and apply regulatory guidelines/developments and industry
standards/best practices on statistics and SAS programming*

Contribute to the development and implementation of internal process
improvement initiatives








Thanks & Regards,

Rasheed
Hamsol Technologies LLC
Email: rasheedham...@gmail.com

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