*Hi*

*Please go through the below position and if you feel comfortable, then
please send me your updated resume*



*Position    : **Senior SAS Programmer *

*Location   : **New Jersey*

*Duration  : 12+ Months*

*Interview : phone then Skype*



*Need clinical SAS Programmers in NJ that knows CDISC, Tables listings,
figures, for clinical trials.*




*Main Responsibilities:*

- Write SAS programs to generate derived analysis datasets, perform
analysis, and TFLs.
- Expertise in the use of SAS (Macros, SQL, efficient Programming) and
other in-house reporting systems
- Perform ad hoc flexible and rapid programming arising from questions
generated from planned analyses and results.
- Ensure consistency and adherence to standards within their therapeutic
area.
- To be responsible for developing, maintaining and validating standard
data structure and software
- Provide programming support for the preparation of integrated reports,
submissions and post-submission activities.

*Skills/Knowledge Required:*

- Bachelor's degree in life science, statistics, mathematics, computer
science, or related field is required; Master's degree is preferred.
- 6 plus years Pharmaceutical/CRO experience as a SAS Programmer
- Organization, time management and attention to detail skills needed to
work - in a stressful environment under tight deadlines while maintaining
focus on details and quality.
- Good knowledge of statistical terminology, clinical tests, medical
terminology, and protocol designs.
- Demonstrated ability to work in a team environment with clinical team
members.









*Ankush Nirala* | Technical Recruiter | Apetan Consulting LLC

Tel: 201- 620- 9700* 112 | Mail: 72 Van Reipen Avenue # 255 Jersey City, NJ
07306 |

Corp.Office: 15 Union Avenue,  office # 6,  Rutherford, New Jersey 07070 |

[email protected] | G-talk: [email protected] | www.apetan.com

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