Hi ,
Greetings for the Day!!!!....
This is *David *from *Ramsoft Inc.* Hope you are doing well and appreciate
for your response. We have a very good openings for *Sr. SAS Clinical
with Macro Exp* Positions with our *Direct Client.*
Please go through that and revert me with your word formatted profile along
with below mentioned details to *[email protected]
<[email protected]> / [email protected]
<[email protected]> :*
*Sr. SAS Clinical with Macro Exp*
*Location NJ, F2F required*
*6+ months*
*JD:*
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. Serve as the lead programmer in support of NDAs, sNDAs.
7. Oversee the services provided by CROs.
8. Contribute to the creation, maintenance, and validation of standards for
programming tools, outputs and macros.
9. Provide training on departmental SOPs/WPs and standard programs.
10. Contribute to the creation of naming conventions and standards for the
programming environment.
11. Participate in industry wide technical discussions.
*Skills/Knowledge Required: *
* Bachelor's degree in life science, statistics, mathematics, computer
science, or related field is required; Master's degree is preferred.
* 9 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting
clinical trials for regulatory submissions with a Bachelor's degree; or 8
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.
* Excellent planning and project management skills.
* Good interpersonal, communication, writing and organizational skills.
* Keep abreast of evolving regulatory, industry, and technology changes and
demands, e.g., CDISC, SDTM, ADaM, eDC.
-
Thanks & Regards,
David
Email: [email protected] / [email protected]
Tel: 732-666-0014
Fax: (480) 393 4994
Web: www.ramsoftinc.com
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