Hi There

Hope you are doing great

I have an urgent requirement for which I am sending you the job
description, please go through the requirement, if you feel interested
please reply with your updated resume.

*REQUIREMENT DETAILS:*

Sr. Biostatistician Req (Clinical SAS Programmer)

Woodcliff Lake, NJ

Rate: $60/hr – C2C

F2F interview will be required after positive phone interview

Duration: 1 year



   - Work closely with clinicians, programmers, and publication managers to
   generate and QC outputs for publications; review publication
   (abstract/manuscripts) to ensure accuracy, quality and soundness of
   statistical methodologies; coordinate internal resource utilization for
   publication and generate activities metrics for management review.
   - Work with the clinical study team on study design, development and/or
   review of clinical study protocols.
   - Develop and/or review statistical analysis plans, including
   Table/listing/figure shells, and final study report for clinical studies;
   perform post-hoc statistical analyses as needed.
   - Work with the project statistician and clinical data managers on
   design/review of case report form, data transfer specification, edit check
   specification, and participation in user acceptance testing (UAT);
   generate/review data tables/listings and coordinate data review meetings
   during the course of the study to ensure data quality.
   - Oversee CRO programming activities, perform quality assurance checks
   on internally or externally produced SAS tables, listings, and figures,
   ensure the quality of CRO deliverables.
   - May work with the Health Outcome team on the
   design/analysis/validation of projects.
   - May work on submission teams as a statistician and/or a programmer.
   - About 55% programming and 45% statistician tasks

*QUALIFICATIONS NEEDED:*

   - Must have a MS in Biostatistics/Statistics with at least 5 years of
   experience or a PhD in Biostatistics/ Statistics with at least 3 years of
   experience in the pharmaceutical, CRO or biotech industry.
   - Strong SAS programming skills.
   - Oncology experience is highly preferred.
   - Good technical writing skills.
   - Good communication skills (verbal and written).
   - Strong teamwork ability/commitment and individual initiative.
   - Strong organizational skills with ability to effectively manage
   multiple projects.

We need is an experienced statistician who can do SAS programming at the
same time can clearly interprets statistical concept and results to
non-statisticians and key medical opinion leaders

The manager prefers candidates with more than 7 years of programming
experience. The manager is seeking a STRONG STATISTICIANS/PROGRAMMERS...the
doers not management. They should have more than 7 years Programming
experience . 25+ years experience will be rejected.

*Thanks & Regards*

*Swati Pandit*

*Technical Recruiter*

*Sage Group Consulting, Inc*

*W:+ 732-767-0010 x 504 |Email: **span...@sagetl.com* <r...@sageci.com>

*Gtalk: svsswa...@gmail.com <svsswa...@gmail.com>*

*Yahoo: svsswa...@yahoo.com <svsswa...@yahoo.com>*

*www.sageci.com <http://www.sageci.com>*

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